anti-rabbit secondary antibody review

This is a Validated Antibody Database (VAD) review about anti-rabbit secondary antibody, based on 216 published articles (read how Labome selects the articles), using anti-rabbit secondary antibody product in experiments. It is aimed to help Labome visitors find the most suited anti-rabbit secondary antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.

Biomeda goat anti-rabbit IgG Cy3 conjugate was used in 1:500 to perform immunohistochemistry in order to show that host-bacterial mutualism in the intestine is protected from immune system by antibacterial lectin RegIIIgamma to the paper

eBioscience TrueBlot anti-rabbit Ig IP Beads was used to perform co-immunoprecipitation assay in order to study the interaction of Ffh or FtsY with s32 to the paper

eBioscience secondary anti-rabbit TrueBlot antibody was used to perform western blot in order to show that cell compartment-specific immune response of Arabidopsis induced by pathogen needs EDS1 as a connector to the paper

InvitrogenInvitrogen anti-rabbit secondary antibody productshown:30; total:106

Molecular Probes Alexa Fluor 546 goat anti-rabbit IgG was used to perform immunocytochemistry in order to show the role of cell adhesion and cortex tension in cell sorting during gastrulation A-11010 to the paper

Pierce anti-Rabbit HRP was used to perform western blot in order to explore the role for the cytoplasmic aggregation process in the molecular pathology of Huntington's disease 32460 to the paper

Invitrogen Alexa Fluor 585 goat anti-rabbit IgG was used to perform immunohistochemistry in order to show that ethylene could induce ER-tethered EIN2 processing and translocation to the paper

Goat anti-rabbit AlexaFluor-555 secondary antibody was used for immunofluorescence assay, in order to study the role of Huntingtin in apical polarity during the morphogenesis of the mouse mammary epithelium to the paper

Rabbit Alexa-488 IgG antibody was used in immunofluorescence detection in macrophages in order to study the acid-dependent secretion process during Salmonella macrophage infection to the paper

Alexa 488-conjugated goat anti-rabbit IgG was used in immunohistochemical assay in order to study the role of intracellular polarity in myelination and remyelination to the paper

Alexa Fluor 647-conjugated antibody to rabbit IgG was used to detect CFL1 or ADF in brain sections in order to study the role of cofilin1 in transcolumnar plasticity in dendritic spines in adult barrel cortex to the paper

Alexa Fluor 568 goat anti-rabbit antibody was used in order to investigate the role of disinhibitory circuit in regulating adult cortical plasticity to the paper

chicken anti-rabbit Alexa Fluor 647 was used for live cell imaging, in order to study the role of Bub1 in the process of spindle assembly checkpoint to the paper

Molecular Probes alexa fluor 488 goat antirabbit was used to perform immunohistochemistry in order to study mammalian olfactory system to the paper

Pierce HRP-conjugated anti-rabbit antibody was used to perform western blot in order to study the regulation mechanism of the cell division by DidA in Caulobacter crescentus to the paper

Invitrogen HRP-conjugated goat anti-rabbit antibody was used to perform immunohistochemistry in order to study the compositions of a sleep-stabilizing pathway in Drosophila to the paper

Invitrogen donkey anti-rabbit 555 was used to perform immunohistochemistry in order to study the significance of DATILOGRAFO in specific cholinergic neurons for sexual receptivity in Drosophila females to the paper

Molecular Probes anti-rabbit 680 was used to perform western blot in order to study the stuctural basis for the linkage between the dynein motor with a cargo-binding region to the paper

Molecular Probes Alexa Fluor 488-conjugated donkey anti-rabbit IgG was used to perform immunohistochemistry in order to study the role of Dmxl2 in the infertility associated with a loss of GnRH neurons in mouse to the paper

Invitrogen Alexa488-coupled anti-rabbit IgG was used to perform immunohistochemistry in order to study the regulation mechanism of embryonic tissue separation by combinations of specific ephrin ligand/Eph receptor pairs to the paper

Invitrogen Alexa Fluor 488 donkey anti-rabbit was used to perform immunohistochemistry in order to study the mechanism by which the small molecule inhibitor of TGF-beta receptor I (Alk5) reverses beta cell de-differentiation to the paper

Life Technologies goat anti-rabbit IgG Alexa Fluor488 was used to perform immunohistochemistry in order to study the effect of histone supply on S phase timing and cell cycle progression to the paper

Invitrogen Alexa 488-conjugated donkey anti-rabbit was used to perform immunohistochemistry in order to study the mechanism of the action potential initiation in neocortical inhibitory interneurons to the paper

Invitrogen Alexa Fluor 568-conjucated anti-rabbit IgG was used to perform immunocytochemistry in order to study the interaction between TLR and Siglec families of pattern recognition receptors and its regulation to the paper

Invitrogen anti-rabbit Alexa Fluor conjugate was used to perform immunohistochemistry in order to study the mechanism by which the cross-synaptic synchrony shapes retinal responses to physiological light inputs and signaling in complex neural networks to the paper

Life Technologies Alexa Fluor 488-conjugated goat anti-rabbit was used to perform immunocytochemistry in order to study the effect of the histone H3K23 methylation on DNA damage in pericentric heterochromatin during meiosis to the paper

Molecular Probes alexa's 647 conjugated anti-rabbit was used to perform immunocytochemistry in order to study the distinct roles for wnt signalling in the specification of spinal cord and paraxial mesoderm identity to the paper

Molecular probes donkey anti-rabbit Alexa 488 was used to perform immunofluorescence in order to study Nodal expression regulates differentiation of epiblast cells to the paper

Life Technologies Alexa-488 goat-anti-rabbit secondary antibody was used to perform immunofluorescence in order to study the morphogenesis of Stentor to the paper

Molecular Probes AlexaFluor 488 or 568-conjugated anti-rabbit antibodies were used to perform immunohistochemistry in order to study brain endothelial cells control reproduction through Semma3A-Nrp1 signaling to the paper

Invitrogen anti-rabbit secondary antibody was used to perform immunohistochemistry in order to study the mechanism of cell elongation to the paper

Invitrogen anti-rabbit IgG secondary antibody was used to perform immunohistochemistry in order to study synaptic plasticity to the paper

Invitrogen Alexa Fluor 555 goat anti-rabbit antibody was used to perform flow cytometry in order to study the role of type I interferons in the DC maturation after poly IC stimulation to the paper

Molecular Probes goat anti-rabbit secondary antibody was used to perform immunocytochemistry in order to explore the effect of the neuregulin and BDNF on NMDA receptor-dependent myelination by oligodendrocytes to the paper

Jackson ImmunoResearch Laboratoriesshown:30; total:50

Jackson ImmunoResearch donkey anti-rabbit-Cy3 was used to perform immunohistochemistry in order to investigate the roles of VAL- and TMT-opsins in neuronal photoreception in medaka fish and zebrafish 711-165-152 to the paper

Jackson ImmunoResearch Cy-3 conjugated donkey anti-rabbit IGG was used to perform immunohistochemistry in order to study the mechanism by which Caenorhabditis elegans discriminates familar food from novel food and increases feeding response to familiar food 711-165-152 to the paper

Rhodamine Red-X goat anti-rabbit antibody was used for cell immunostaining in order to study the effects of aneuploidy on chromosome mis-segregation and cytokinesis failure to the paper

Dylight 649 goat anti-rabbit Fab fragment was used for KIF1C single molecule assay, in order to study the function of Rab6A binding to KIF1C's motor domain to the paper

Jackson ImmunoResearch peroxidase-conjugated Affinipure goat anti-rabbit IgG (H+L) was used to perform western blot in order to study therole of the human lariat RNA debranching enzyme 1 protein in both the nucleus and the cytoplasm to the paper

goat anti-rabbit RRX was used for live cell imaging, in order to study the role of Bub1 in the process of spindle assembly checkpoint to the paper

Jackson ImmunoResearch Cy3 anti-rabbit IgG was used to perform immunohistochemistry in order to study the mechansim of the glial responsiveness to axonal injury in Drosophila to the paper

Jackson Immuno Research HRP-conjugated goat anti-rabbit IgG was used to perform western blot in order to study the generation mechanism of Peroxisomal lactate dehydrogenase in mammals to the paper

Jackson ImmunoResearch donkey anti-rabbit Cy3 conjugate secondary antibody was used to perform immunofluorescence in order to study Ryk-ICD pathway in mutant polyglutamine neurons to the paper

Jackson ImmunoResearch anti-rabbit Cy3 secondary antibody was used to perform immunohistochemistry in order to study how opposing motor programs coordinate feeding and locomotive behaviors to the paper

Jackson anti-rabbit-Cy3 secondary antibody was used to perform immunohistochemistry in order to study zebrafish neural crest migration to the paper

Jackson ImmunoResearch goat anti-rabbit IgG FITC conjugate was used to bind with phosphoH3-S10 antibody for the analysis of G2/M checkpoint in order to study the role of RSFI in DSB repair to the paper

Jackson ImmunoResearch anti-rabbit antiboy was used to perform immunohistochemistry in order to study the role of the retromer in recycling rhodopsins to maintain PR function and integrity to the paper

Jackson ImmunoResearch Laboratories anti-rabbit IgG secondary antibody was used to perform immunohistochemistry in order to study synaptic plasticity to the paper

Jackson ImmunoResearch Cy3-conjugated anti-rabbit secondary antibody was used to perform immunohistochemistry to study the effect of mast cells with A20 deficiency on inflammatory responses to the paper

Jacksons Immunoresearch Cy3-conjugated donkey anti-rabbit was used to perform immunohistchemistry in order to study the role of BMP signaling pathway in setting the circadian period in PDF neurons in the adult brain to the paper

Jackson ImmunoResearch peroxidase-conjugated affinipure goat anti-rabbit IgG (1:10,000) was used to perform western blot in order to study the role for TRAF4, a novel phosphoinositide-binding protein, in modulating tight junctions and promoting cell migration to the paper

Jackson Immunoresearch Cy5-conjugated donkey anti-rabbit antibody was used to perform flow cytometry in order to investigate the role of hybrid Th1/2 cells in natural immune responses against parasites to the paper

Jackson ImmunoResearch Cy5-donkey anti-rabbit antibody was used to perform immunohistochemistry in order to investigate the role of CDON in regulating tumor cell survival to the paper

Jackson ImmunoResearch allophycocyanin-donkey anti-rabbit IgG was used to perform flow cytometry in order to investigate the regulatory mechanism of RasGRP1 to the paper

Jackson ImmunoResearch Laboratories horseradish peroxidase-conjugated donkey anti-rabbit IgG was used to perform western blot in order to investigate the influence of resveratrol on mitochondrial biogenesis in muscle to the paper

Jackson ImmunoResearch DyLight 488-conjugated Affini-Pure Goat anti-rabbit IgG was used to perform immunohistochemistry in order to investigate the mechanism of tip link regeneration in auditory hair cells to the paper

Jackson Immunoresearch Cy3-conjugated anti-rabbit antibody was used to perform immunofluorescence in order to study the contributions of mast cells to dengue virus-induced vascular leakage to the paper

Jackson Immunoresearch Cy3-conjugated anti-rabbit IgG (dilution, 1:1,000) was used to perform immunofluorescence in order to study whether pheromonal ligands are conformationally activated odorant binding proteins to the paper

Jackson ImmunoResearch Cy3 goat anti-rabbit antibody was used to perform immunohistochemistry assays in order to investigate the role of Rac in the regulation of niche-associated polarity during the asymmetric division of Drosophila female germline stem cells to the paper

Jackson Immuno Research secondary antibodies peroxidase-conjugated Goat anti-rabbit IgG were used to perform western blot in order to show that lac repressor binds with sequence-specific sites using facilitated diffusion manner in living cells to the paper

Jackson ImmunoResearch HRP-conjugated donkey anti-rabbit Ig was used to perform immunohistochemistry in order to show that fetomaternal immune tolerance was regulated by chemokine gene silence in decidual stromal cells to the paper

Jackson ImmunoResearch horseradish-peroxidase conjugated donkey anti-rabbit IgG was used to perform immunohistochemistry in order to show that axon death activated by injury needs dSarm/Sarm1 signal to the paper

Jackson Rhodamine Red-X labeled anti-rabbit secondary antibody was used to perform immunocytochemistry in order to investigate the regulatory effect of Ca2+ influx through TRPV4 cation channels on vascular function to the paper

Jackson ImmunoResearch Cy3 conjugated donkey anti-rabbit secondary antibody was used to perform immunocytochemistry in order to investigate the importance of Dilp8 in regulation of Drosophila tissue growth to the paper

AbcamAbcam anti-rabbit secondary antibody product

Abcam normal rabbit IgG was used to perform Co-IP in order to study the function of eEF1A1 in transcription during heat shock response to the paper

Bio-RadBio-Rad anti-rabbit secondary antibody product

Serotec phycoerythrin-conjugated sheep anti-rabbit IgG was used to perform flow cytometric analysis in order to illustrate that Toll-like receptor 4 (TLR4) plays a fundamental role in the sensing of LPS from Gram-negative bacteria to the paper

Rockland ImmunochemicalsRockland Immunochemicals anti-rabbit secondary antibody product

Horseradish peroxidase-conjugated antibody to rabbit IgG was used to perform in vitro KD experiments in order to study the role of cofilin1 in transcolumnar plasticity in dendritic spines in adult barrel cortex to the paper

Rockland Immunochemicals Inc. anti-rabbit IgG beads was used to perform immunoprecipitation in order to study the morphogenesis of Stentor to the paper

Rockland anti-rabbit IgG antibody was used to perform western blot in order to study the function of chemokine GPCR signaling in the formation of zebrafish axis to the paper

Dianova

Dianova rabbit-antiGFP Cy2 secondary antibody was used to perform immunohistochemistry in order to study how opposing motor programs coordinate feeding and locomotive behaviors to the paper

Dianova anti-rabbit coupled to horseradish peroxidase was used in 1:20000 to perform western blot in order to show that in Drosophila centromere formation could be induced by CENH3 to the paper

Dianova biotin-conjugated donkey anti-rabbit IgG was used to visualize specific antibody in order to study if targeteddisruption of Slc2a8 (GLUT8) reduces motility and mitochondrial potential of spermatozoa to the paper

Boster

Boster BioTec HRP-goat anti-rabbit IgGantibody was used to examine microvessels in tumors by immunohistochemical staining to investigate the change of tumor angiogenesis in RBP-J knockout mouse to the paper

Active Motif

Active Motif anti-rabbit Chromeo 494 was used to perform immunohistochemistry in order to show that normal brain development needs microglia-mediated synaptic pruning to the paper

Agrisera

Agrisera goat anti-rabbit IgG was used to perform western blot in order to study the mechanism by which one trihelix DNA binding protein regulates hypoxia-responsive transcriptional activation in Arabidopsis to the paper

Santa Cruz Biotechnology

Anti-rabbit secondary antibody was used in immunoblotting assay in order to study the acid-dependent secretion process during Salmonella macrophage infection to the paper

HRP conjugated anti-rabbit antibody was used for immunoassay, in order to demonstrate engineering of electrically and chemically responsive, contractile human muscle tissues using primary myogenic cells to the paper

Santa Cruz Biotechnology Horseradish perioxidase conjugated anti-rabbit was used to perform western blot in order to study the interaction between TLR and Siglec families of pattern recognition receptors and its regulation to the paper

Santa Cruz Biotechnology HRP-conjugated goat anti-rabbit secondary antibody was used to perform western blot in order to investigate the functional property of the CK2 kinase in Drosophila to the paper

Santa Cruz Biotech horseradish peroxidase-conjugated goat anti-rabbit IgG secondary antibody was used to perform western blot in order to investigate the role of the mGluR5-Erk pathway in tuberous sclerosis complex to the paper

Santa Cruz biotechnology HRP-conjugated goat anti-rabbit antibody was used to carry out western blot analysis in order to determine the role of CULLIN-3 in the control of TIM oscillations in the Drosophila circadian clock to the paper

Santa Cruz Biotechnology non-specific rabbit IgG was used to perform ChIP assay in order to show that fetomaternal immune tolerance was regulated by chemokine gene silence in decidual stromal cells to the paper

Santa Cruz Biotechnology rabbit anti-HA antibody was used to perform western blot and immunoprecipitation in order to investigate the role of GSK3-TIP60-ULK1 signaling pathway in autophagy to the paper

Santa Cruz HRP-labeled anti-rabbit secondary antibody was used to perform western blot in order to show that vacuolar H+-ATPase is involved in mTOR pathway for mTORC1 translocation and activation to the paper

Santa Cruz Biotechnology goat antimouse and anti-rabbit horseradish peroxidase-conjugated antibodies were used in western blot in order to show that Parp1 and ADP-ribose polymers localize on the Dnmt1 promoter and Parp1 can protect its unmethylated state to the paper

Santa Cruz Biotechnology rabbit IgG was used to perform chromatin immunoprecipitation in order to illustrate that anthracycline chemotherapy can inhibit the transcription of HIF-1 as well as the mobilization of circulating angiogenic cells in tumor to the paper

Santa Cruz anti-rabbit IgG antibody was used for western blot in order to investigate the role of transcription factor Ets-1 in the regulation of Natriuretic Peptide Receptor-A expression to the paper

MilliporeSigma

Sigma-Aldrich goat anti-rabbit IgG horseradish peroxidase conjugated was used to perform western blot in order to study the effect of histone supply on S phase timing and cell cycle progression to the paper

Sigma control rabbit IgG antibody was used to perform RNA ChIP in order to show that PER complex could regulate transcriptional termination directly to the paper

Sigma anti-rabbit IgG was used to perform western blot in order to show that histone mRNA 3 end processing needs the phosphorylation of RNAP II CTD Thr4 to the paper

SIGMA anti-rabbit gold-10nm conjugate was used in 1/50 to perform immunogold staining in order to show that insect endosymbionts could be protected by ColA antimicrobial peptide to the paper

Sigma-Aldrich HRP-conjugated goat anti-rabbit was used to perform western blot in order to show that mitochondrial fission could be mediated by ER tubules to the paper

Sigma anti-rabbit-HRP conjugate was diluted in 1:10,000 and used to perform western blot in order to show that cell-wall synthesis complexes interact with MreB and do processive movement in B. subtilis to the paper

Sigma rabbit IgG was used as a negative control in order to demonstrate that KSHV tegument protein play a crucial role in cellular transport of viral particles to the paper

Sigma FITC-conjugated anti-rabbit IgG was used as secondary antibody in immunostaining in order to research the functions of the matrix metalloproteinase-7 to the CNS in experimental autoimmune encephalomyelitis to the paper

Sigma rabbit anti-Rad50 polyclonal (1:5,000) antibody was used in western blot in order to study the role of Rad50 for the maintenance and viability of postmitotic tissues to the paper

Sigma HRP-conjugated goat anti-rabbit antibody was used to carry out western blot anaylsis in order to investigate the roles of inner tegument proteins pUL36 and pUL37 during entry of Herpes Simplex Virus type 1 to the paper

Sigma FITC-conjugated goat anti-rabbit antibody was used to perform immunofluorescence in order to indicate that the two functions of herpes simplex virus 1 ICP0, the degradation of PML and the blocking of silencing by the CoREST/REST/HDAC complex, are interdependent to the paper

Sigma Aldrich FITC-conjugated goat anti-mouse IgG was used for flow cytometry in order to demonstrate that chemokines could activate human endothelial cell selectively as a guide to cell homing to the paper

Bio-Rad

Bio-rad secondary goat anti-rabbit antibodies conjugated with horseradish peroxidase were used to perform western blot in order to show that ethylene could induce ER-tethered EIN2 processing and translocation 170-6515 to the paper

Bio-Rad Goat anti-rabbit IgG-HRP was used to perform western blot in order to study the effect of a conserved endoplasmic reticulum membrane protein complex (EMC) on phospholipid transfer to the paper

Biorad goat-anti-rabbit IgG was used to perform western blot in order to study Ryk-ICD pathway in mutant polyglutamine neurons to the paper

Bio-Rad HRP-conjugated goat anti-rabbit secondary antibodies were used to perform western blot in order to study the role of a class of cell surface directional motors in gliding motility and sporulation in Myxococcus xanthus to the paper

Bio-Rad anti rabbit-HRP was used as secondary antibody for immunoprecipitation and immunoblotting in order to study the interaction between the vaccinia virus p37 and host proteins associated with LE-derived transport vesicle biogenesis to the paper

LI-COR Biosciences

Li-Cor secondary IRDye 800CW Goat anti-rabbit IgG antibody was used to perform western blot in order to show that MAPK misactivation could be insulated by Ste5 conformational changes 926-32211 to the paper

LI-COR Biosciences goat anti-rabbit IgG IRDye 800 was used to perform western blot in order to study the effect of histone supply on S phase timing and cell cycle progression to the paper

Licor IRDye 680-conjugated goat anti-rabbit antiserum was used to perform western blot in order to study one method of reconstituting bacterial autotransporter assembly using purified components to the paper

LI-COR Biosciences IRDye 680RD goat-anti-rabbit secondary antibody was used to perform western blotting in order to study the morphogenesis of Stentor to the paper

Li-Cor anti-rabbit IgG was used to perform western blot in order to show that histone mRNA 3 end processing needs the phosphorylation of RNAP II CTD Thr4 to the paper

Licor goat anti-rabbit IRDye 680 was used to perform western blot in order to show that vagus nerve circuit could inhibit cytokine production through acetylcholine-producing T cells in spleen to the paper

LI-COR Biosciences donkey anti-rabbit IRDye-800CW was used to perform western blot in order to study the role of the neuronal calcium sensor-1 in the functional plasticity in spinal cord in rats to the paper

Li-Cor Bioscience IRDye 800-conjugated secondary antibodies against mouse, rabbit, and goat IgG were used in western blot and immunoprecipitation in order to explain that PDCD5 can maintain the histone acetyltransferase activity of the Tip60 protein and promote DNA damage-induced apoptosis as a Tip60 coactivator to the paper

Diagenode

Diagenode rabbit-IgG was used to perform ChIP assay in order to show that telomerase was regulated by Wnt/beta-catenin signaling to the paper

Diagenode anti-rabbit Control IgG was used to perform ChIP assays in order to show that cell fate choice could be modulated by chromatin "prepattern" and histone modifiers to the paper

Dako

Horseradish peroxidase-conjugated antibody to rabbit IgG was used to detect CFL1 or ADF in brain sections in order to study the role of cofilin1 in transcolumnar plasticity in dendritic spines in adult barrel cortex to the paper

Dako rabbit anti-mouse secondary antibodies conjugated to horseradish peroxidase were used to perform western blot in order to study the role of the cytosolic C-ring in the Type III secretion injectisome to the paper

Dako anti-rabbit antibody was used to perform western blot in order to explore the effect of the neuregulin and BDNF on NMDA receptor-dependent myelination by oligodendrocytes to the paper

Dako swine anti-rabbit secondary antibody conjugated to horseradish peroxidase was used to perform western blot in order to investigate the structural features of the Yersinia injectisome to the paper

Dako HRP-conjugated anti-rabbit-IgG was used to perform western blot in order to explore the role of glucosylceramide synthase in central nervous system in the regulation of body weight and energy homeostasis to the paper

Dako FITC-labeled swine anti-rabbit IgG antibody was used to perform immunohistochemistry in order to study the secretion of proinflammatory cytokines and generation of Th17 cells induced by IL-26 to the paper

DAKO rabbit anti-Escherichia coli B was used to perform immunohistochemistry in order to show that skin microbiota could provide protective immunity to the paper

DAKO anti-rabbit HRP secondary antibody was used to perform western blot in order to investigate the function of vitamin K2 to the paper

Dako horseradish peroxidase-conjugated goat anti-rabbit was used to perform western blot in order to show that ciliogenesis was regulated by an evolutionarily assembled cis-regulatory module to the paper

DakoCytomation biotin-conjugated anti-rabbit was used to perform immunocytochemistry in order to show that blood-brain barrier integrity and CNS immune quiescence were promoted by sonic hedgehog pathway to the paper

DAKO Goat anti-rabbit-PO was used to perform western blot in order to show that chromosomal structural aberrations could be caused by chromosome segregation errors to the paper

DAKO anti-rabbit EnVision+-HRP-conjugated polymer was used in immunohistochemistry in order to show a novel pathomechanism of muscular dystrophy affecting attenuated muscle regeneration to the paper

DakoCytomotion secondary HRP-conjugated polyclonal goat anti-rabbit antibody was used in western blot in order to study gene dosage effects of the imprinted Dlk1/Pref1 in development and the role of postnatal lethality for its to the paper

Dako anti-rabbit horseradish peroxidase-conjugated secondary antibodies were used for western blot in order to illustrate the new functions of SAP30L and SAP30 in mediating key protein-protein and protein-DNA interactions involved in chromatin remodeling and transcription to the paper

New England Biolabs

Invitrogen Alexa-labeled anti-rabbit secondary antibody was used to perform immunocytochemistry in order to study the roles of kif2a and importin alpha in the spindle scaling during Xenopus embryogenesis to the paper

Cell Signaling Technology

Alexa Flour 647 Goat anti-Rabbit antibody was used for immunoblot, in order to study the function of Rab6A binding to KIF1C's motor domain to the paper

Cell signaling anti-rabbit secondary antibody was used to perform western blotting in order to study type III interferon (IFN) suppresses tumor growh to the paper

Cell Signaling Technology Alexa Fluor 488 goat anti-rabbit IgG was used to perform immunocytochemistry in order to investigate the regulatory effect of HILDA complex on VEGF-A expression to the paper

Cell Signaling Technologies.anti-rabbit antibody conjugated to HRP was used for western blot in order to analyze the functional domains of Epstein-Barr Virus Glycoprotein B to the paper

GE Healthcare Life Biosciences

HRP-conjugated goat anti-mouse antibody was used in Western blotting assay, in order to study the role of Huntingtin in apical polarity during the morphogenesis of the mouse mammary epithelium to the paper

anti-rabbit antibody was used for western blotting, in order to study the role of Bub1 in the process of spindle assembly checkpoint to the paper

GE Healthcare anti-rabbit horseradish peroxidase-linked secondary antibody was used to perform western blot in order to study the stuctural basis for the linkage between the dynein motor with a cargo-binding region to the paper

GE-Healthcare horseradish peroxidase-conjugated goat-anti-rabbit was used to perform western blot in order to study the function of eEF1A1 in transcription during heat shock response to the paper

GE Life Sciences HRP-conjugated alpha-rabbit secondary antibody was used to perform ELISA assay in order to study the effect of the histone H3K23 methylation on DNA damage in pericentric heterochromatin during meiosis to the paper

Amersham Biosciences donkey anti-rabbit diluted in 1:10,000 was used to perform western blot in order to show that cognitive deficits of Alzheimer's disease model could be reversed by STEP inhibitor to the paper

AbD Serotec HRP-conjugated goat anti-rabbit IgG was used to perform immunohistochemistry in order to study synaptic plasticity to the paper

GE healthcare anti-rabbit IgG was used to perform immunoprecipitation in order to investigate the regulatory effect of HILDA complex on VEGF-A expression to the paper

GE Healthcare anti-rabbit IgG horseradish peroxidase secondary antibody was used to perform western blot in order to study the mechanism by which Wnt signaling pathways regulate the specification and patterning of the neuroectoderm in sea urchin embryos to the paper

GE Healthcare HRP-labeled anti-rabbit IgG was used to perform western blot in order to show that a sharp boundary in chordate embryos was established by cis-acting transcriptional repression to the paper

GE Healthcare donkey anti-rabbit-HRP was used to perform western blot in order to study the effect of one Toxoplasma gondii pseudokinase on the host IRG resistance proteins to the paper

GE Healthcare horseradish peroxidase-conjugated anti-rabbit was used to perform western blot in order to show that protein could be synthesized using CUG as start codons to provide peptides for MHC class I to the paper

GE HealthCare anti-rabbit IgG-HRP-conjugated donkey antibody was used at 1:1000 to perform immunostaining in order to show that dorsal aorta is essential for sympatho-adrenal specification to the paper

GE healthcare anti-rabbit IgG-HRP was used to perform ELISA in order to show that yeast could be used to model Abeta toxicity for potential modifier screen to the paper

GE Healthcare ECL rabbit IgG, HRP-Linked Whole Ab from donkey was used in 1:2000 to perform western blot in order to show that stochastic pulse frequency could be regulated by environmental stress through alternative sigma factor in bacteria to the paper

GE Healthcare Cy5-labeled goat-anti-rabbit was used to perform western blot in order to show that H-NS could promote chromosome organization in bacteria to the paper

GE Healthcare HRP-conjugated anti-rabbit antibodies were used to perform western blot in order to show that axonal projection could be regulated by cartilage acidic protein-1B through NgR1 inhibition to the paper

GE Healthcare HRP conjugated anti-rabbit antibody was used in western blot in order to demostrate that the target gene expression can be promoted through Smad2/3 activation to the paper

Amersham horseradish peroxidase-conjugated sheep anti-rabbit secondary antibody was used to perform immunoprecipitation in order to study the effect of gE/gI heterodimer formation on efficient cell-cell spread to the paper

Biocare Medical

BioCare Medical HRP anti-rabbit secondary antibody was used to perform immunohistochemistry in order to study the mechanism by which de-differentiation confers multidrug resistance to the paper

Promega

Promega goat anti-IgG rabbit secondary antibody was used to perform protein blot in order to study whether pheromonal ligands are conformationally activated odorant binding proteins to the paper

Promega alkaline phosphatase labeled goat anti-rabbit IgG (H+L) was used to perform ELISA in order to show that Pf sporozoites specific CD8+ could be induced by live attenuated malaria vaccine to the paper

Vector Laboratories

Vector Laboratories biotinylated goat anti-rabbit was used at 1:200 to perform immunohistochemistry in order to show that mucosal innate immunity could be promoted by HD6 self-assembly to the paper

Vector Labs goat anti-rabbit IgG was used at 1:5000 to perform western blot in order to show that drug craving could be inhibited through a specific memory treatment to the paper

Vector labs anti-rabbit-biotin was used in 1/300 to perform immunohistochemistry in order to show that neuroinflammation could be promoted by prostaglandin generated from endocannabinoid hydrolysis to the paper

Vector laboratories biotinylated goat anti-rabbit secondary antibody was used to perform immunohistochemistry in order to show that synaptic efficacy in mPFC is associated with social hierarchy to the paper

Vector biotinylated anti-rabbit IgG was used to perform immunohistochemistry in order to show that inflammatory arthritis mice model could be treated by progranulin through interaction with TNF receptor to the paper

Vector Laboratories anti-rabbit peroxydase-conjugated antibody was used to perform immunohistochemistry in order to demonstrate that neoplastic cells of several B-cell lymphomas and tumor-associated macrophages can express the immunosuppressive enzyme IL4I1 to the paper

Vector Laboratories Texas Red-conjugated anti-rabbit IgG was used to perform immunofluorescence assays in order to demonstrate that KSHV tegument protein play a crucial role in cellular transport of viral particles to the paper

Vector Laboratories goat anti-rabbit IgG antibody was used to incubate the acetone-fixed sections of the ascending aorta in order to suggest that T-cell activation can limits collagen maturation in the atherosclerotic plaque to the paper

EMD MilliporeEMD Millipore anti-rabbit secondary antibody product

Millipore anti-rabbit Alexa-594 secondary antibodies were used at 1:200 to perform immunostaining in order to show that DNA demethylation could be regulated by IDM1 in Arabidopsis to the paper

Millipore HRP-conjugated anti-rabbit secondary antibody was used to perform western blot in order to investigate the important roles of DILP8 in regulation of peripheral tissue growth in Drosophila to the paper

BD Biosciences

Southern Biotech anti-rabbit IgG-Al488 antibody was used to perform flow cytometry in order to investigate the importance of phosphatase activity in B cell selection in germinal centers to the paper

BD FITC conjugated-anti-rabbit secondary antibody was used to perform immunocytochemistry in order to investigate the importance of acetylation in autophagy regulation to the paper

BD Biosciences FITClabeled goat anti-rabbit was used to perform flow cytometry in order to show that blood-brain barrier integrity and CNS immune quiescence were promoted by sonic hedgehog pathway to the paper

BD PharMingen FITC-conjugated anti-rabbit IgG antibody was used to carry out immunocytochemistry assays in order to analyze the subcellular localization of LRRK2 to the paper

BD Pharmingen FITC-conjugated goat anti-rabbit IgG was used for flow cytometry in order to demonstrate that chemokines could activate human endothelial cell selectively as a guide to cell homing to the paper

Interchim

Interchim FP546-conjugated goat anti-rabbit antibody was used to carry out immunohistochemistry assays in order to determine the role of CULLIN-3 in the control of TIM oscillations in the Drosophila circadian clock to the paper

BBI Solutions

BB International Immuno-gold Conjugate EM Goat F(ab')2 anti-rabbit IgG:10 nm was used to perform immunoelectron microscopy in order to investigate the mechanism of tip link regeneration in auditory hair cells to the paper

Polysciences

Polysciences goat anti-rabbit IgG magnetic beads were used to immunoprecipitate SIRT2-Flag in immunoprecipitation to study SIRT2's interaction with FOXO1 in order to illustrate the suppression of adipocyte differentiation performed by SIRT2 to the paper

Ted Pella

Ted Pella gold-conjugated goat anti-rabbit secondary antibody was used to perform immunohistochemistry in order to study the regulation of the Teneurins on Synaptic organization of the Drosophila antennal lobe to the paper

Kirkegaard & Perry Laboratories

KPL horseradish peroxidase (HRP)-conjugated goat anti-rabbit secondary antibody was used to perform western blot in order to show that mucosal innate immunity could be promoted by HD6 self-assembly to the paper

Aurion

Aurion goat anti-rabbit ultrasmall gold was used to perform immuno-electron microscopy in order to investigate the structural composition of caveolar coat complex to the paper

Boehringer Mannheim

Boehringer Mannheim goat anti-rabbit IgG was used to perform immunocytochemistry in order to study Ryk-ICD pathway in mutant polyglutamine neurons to the paper

Articles Reviewed

Elias S, McGuire J, Yu H, Humbert S. Huntingtin Is Required for Epithelial Polarity through RAB11A-Mediated Apical Trafficking of PAR3-aPKC. PLoS Biol. 2015;13:e1002142 pubmed publisher
Nicholson J, Macedo J, Mattingly A, Wangsa D, Camps J, Lima V, et al. Chromosome mis-segregation and cytokinesis failure in trisomic human cells. elife. 2015;4: pubmed publisher
Chakraborty S, Mizusaki H, Kenney L. A FRET-based DNA biosensor tracks OmpR-dependent acidification of Salmonella during macrophage infection. PLoS Biol. 2015;13:e1002116 pubmed publisher
Lee P, Ohlson M, Pfeffer S. Rab6 regulation of the kinesin family KIF1C motor domain contributes to Golgi tethering. elife. 2015;4: pubmed publisher
Jarjour A, Boyd A, Dow L, Holloway R, Goebbels S, Humbert P, et al. The polarity protein Scribble regulates myelination and remyelination in the central nervous system. PLoS Biol. 2015;13:e1002107 pubmed publisher
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