anti-mouse IgG H+L secondary antibody review

This is a Validated Antibody Database (VAD) review about anti-mouse IgG H+L secondary antibody, based on 192 published articles (read how Labome selects the articles), using anti-mouse IgG H+L secondary antibody product in experiments. It is aimed to help Labome visitors find the most suited anti-mouse IgG H+L secondary antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.

eBioscience TrueBlot ULTRA anti-mouse IgG-HRP was used to perform western blot in order to investigate the functional property of the CK2 kinase in Drosophila to the paper

InvitrogenInvitrogen anti-mouse IgG H+L secondary antibody productshown:30; total:97

Molecular Probes Alexa Fluor 546 Goat anti-Mouse IgG (H+L) was used to perform immunocytochemistry in order to show the role of cell adhesion and cortex tension in cell sorting during gastrulation A-11003 to the paper

Invitrogen anti-mouse Alexa Fluor 555 antibody was used to perform immunocytochemistry in order to study RAS/MAPK Signaling control transcription and splicing in Drosophila A-21424 to the paper

Invitrogen Alexa Flour 680-conjugated goat anti-mouse antibody was used to perform western blot in order to investigate influenza nucleoprotein evolution A-21058 to the paper

Goat anti-mouse AlexaFluor-488 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

Alexa 488 goat anti-mouse antibody was used for cell immunostaining in order to study the effects of aneuploidy on chromosome mis-segregation and cytokinesis failure to the paper

Alexa 568-conjugated donkey anti-mouse 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 mouse IgG was used to detect MAP2 or NeuN 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-568 conjugated anti-mouse secondary antibody was used for immunoassay, in order to study the role of GTPase Rab26 in directing synaptic and secretory vesicles into the autophagy pathway to the paper

Molecular Probes alexa fluor 555 goat antimouse was used to perform immunohistochemistry in order to study mammalian olfactory system to the paper

Pierce HRP-conjugated anti-mouse 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 Alexa-488 goat anti-mouse was used to perform immunohistochemistry in order to study the compositions of a sleep-stabilizing pathway in Drosophila to the paper

Life Technologies anti-mouse IgG conjugated to Alexa 488 was used to perform immunocytochemistry in order to study the regulation of the Fringe proteins on Notch-ligand cis and trans interactions to specify signaling states to the paper

Life Technologies goat anti-mouse IgG coupled to 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 555-conjugated donkey anti-mouse 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 488-conjugated goat anti-mouse secondary was used to perform immunocytochemistry in order to study the mechanism by which the mother-daughter asymmetry of pH regulates aging and rejuvenation in yeast to the paper

Life Technologies Alex Fluor 647-conjugated goat anti-mouse 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 488 conjugated anti-mouse 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

Invitrogen AlexaFluor 488 conjugated goat anti-mouse secondary antibodies were used to perform immunocytochemistry in order to show that MID gene is critical for sperm and egg development in V. carteri to the paper

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

Life Technologies anti-mouse IgG beads coated with anti-p28 mouse monoclonal antibody were used to purify ookinetes in order to perform biochemical analysis and Ca2+ assays to the paper

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

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

Molecular Probes donkey anti-mouse AlexaFluor488 was used to perform immunohistochemistry to study the regulation of BMP-dependent cardiac contraction by 3-O-sulfotransferase to the paper

Molecular Probes goat anti-mouse Alexa555 was used to perform immunohistochemistry in order to study the role of Smurf proteins in controlling Hh signaling to the paper

Life Technologies Alexa-568 anti-mouse secondary antibody was used to perform immunocytochemistry in order to investigate the importance of the regulation of matrimony levels to the oocyte-to-embryo transition in Drosophila to the paper

Life Technologies Alexa 594-conjugated goat anti-mouse secondary antibody was used to perform immunohistochemistry in order to investigate the functional property of the CK2 kinase in Drosophila to the paper

Invitrogen Alexa Fluor 594 goat anti-mouse IgG was used to perform immunocytochemistry in order to investigate the mechanism of self-cleavage of MYRF to the paper

Life Technologies anti-mouse Alexa555 antibody was used to perform immunohistochemistry in order to investigate the role of Etv2 in vascular development to the paper

Invitrogen AlexaFluor 680 F(ab') fragment of goat anti-mouse IgG was used to perform western blot in order to investigate the mechanism of the pharmacological activity of PTC124 to the paper

Invitrogen Alexa Fluor 546 goat anti-mouse secondary antibody was used to perform immunohistochemistry in order to investigate the role of sFLT-1 in the maintenance of the avascular photoreceptor layer in mouse models to the paper

R&D SystemsR&D Systems anti-mouse IgG H+L secondary antibody product

R&D Systems mouse IgG was used to perform cell culture in order to investigate the role of PVRL4 in tumor progression MAB004 to the paper

R&D Systems horseradish peroxidase-conjugated anti-mouse IgG antibody was used in 1/10,000 to perform ELISA in order to show that IL-17 immunodeficiency could lead to CMCD HAF007 to the paper

Jackson ImmunoResearch LaboratoriesJackson ImmunoResearch Laboratories anti-mouse IgG H+L secondary antibody productshown:30; total:45

Jackson ImmunoResearch Cy3-conjugated goat anti-mouse antibody was used to perform immunocytochemistry in order to investigate the important role of Rad51p in the formation of RNA-DNA hybrids in budding yeast 115-165-003 to the paper

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

goat anti-mouse 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 FITC anti-mouse 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 ImmunoResearch anti-mouse-Alexa-488 was used to perform immunohistochemistry in order to study the evolution of wrist bones in the dinosaur-bird transition to the paper

Jackson ImmunoResearch Cy3-conjugated donkey anti-mouse 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

Jackson Immuno Research HRP-conjugated donkey anti-mouse 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 anti-mouse DyLight 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

Jackson anti-mouse FITC antibody was used to perform immunocytochemistry in order to study the usage of Poly-Ribo-Seq in translating the small open reading frames to the paper

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

Jackson ImmunoResearch peroxidase-conjugated anti-mouse secondary antibody was used to perform western blot in order to investigate the importance of the regulation of matrimony levels to the oocyte-to-embryo transition in Drosophila to the paper

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

Jackson Immunoresearch laboratories Cy3-conjugated goat anti-mouse IgG antibody was used to perform immunohistochemistry in order to investigate the roles of Vav2 and Vav3 in skin cancer to the paper

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

Jackson HRP-conjugated donkey anti-mouse antibody was used to perform ELISA assays in order to investigate the mechanism of the pharmacological activity of PTC124 to the paper

Jackson Immuno Research goat anti-mouse IgG HRP was used to perform western blot in order to investigate the regulatory effect of calcineurin and CAMKII on the lifespan of Caenorhabditis elegans to the paper

Jackson Immunoresearch goat anti-mouse Cy3 antibody was used to perform immunofluorescence in order to study the different trafficking mechanisms of endosomal Toll-like receptors mediated by UNC93B1 to the paper

Jackson ImmunoResearch Cy3 goat anti-mouse 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-Mouse 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 horseradish-peroxidase conjugated donkey anti-mouse IgG was used to perform immunohistochemistry in order to show that axon death activated by injury needs dSarm/Sarm1 signal to the paper

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

Jackson HRP-conjugated anti-mouse 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

Jackson ImmunoResearch Labs donkey anti-mouse was used to perform western blot in order to show that Nodal and Lefty had different diffusivity to achieve their function to the paper

Jackson ImmunoResearch Cy2-conjugated donkey-anti-mouse IgG was used to perform immunohistochemistry in order to show that planar cell polarity is essential for tissue morphogenesis to the paper

Jackson ImmunoResearch Laboratories Alexa 649-conjugated donkey antimouse antibody was used to perform whole mount staining in order to show that specific myeloid cells derived from the yolk sac to the paper

Jackson ImmunoResearch Cy3 conjugated goat anti-mouse antibody was used to perform immunohistochemistry in order to show that brain inhibitory network could be modulated by dendritic gap junctions to the paper

Jackson Immunoresearch anti-mouse antibody was used to perform immunocytochemistry in order to study the activation of the chromosomal passenger complex on Polo kinase at centromeres to the paper

Jackson Immunolabs donkey anti-mouse Cy3-labelled secondary Ab was used to perform immunocytochemistry in order to show that innate immune response against Listeria and LPS is mediated by TNF which is controlled by iRhom2 regulation of TACE to the paper

Jackson Immunoresearch anti-mouse IgGs was used to perform immunohistochemistry in order to show that blood-brain barrier integrity and CNS immune quiescence were promoted by sonic hedgehog pathway to the paper

Jackson ImmunoResearch anti-mouse DyLight 488 was used in 1:1000 to perform immunohistochemistry in order to show that proper organogenesis needs B-type lamins in mice to the paper

AbcamAbcam anti-mouse IgG H+L secondary antibody product

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

Abcam goat anti-mouse FITC antibody was used to perform immunohistochemistry in order to investigate the functional properties of MORC family ATPases to the paper

BioLegendBioLegend anti-mouse IgG H+L secondary antibody product

Biolegend Pe/Cy7 goat anti-mouse IgG was used to perform flow cytometry in order to investigate the regulatory mechanism of RasGRP1 to the paper

Rockland ImmunochemicalsRockland Immunochemicals anti-mouse IgG H+L secondary antibody product

Rockland anti-mouse-800 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

Rockland anti-mouse secondary antibody was used in 1:10,000 to perform western blot in order to show that yeast could be used to model Abeta toxicity for potential modifier screen to the paper

Rockland goat-anti-mouse IRDye800 was used to perform western blot in order to illustrate that local ATP generation by brain-type creatine kinase (CK-B) could facilitate cell motility to the paper

Active Motif

Active Motif anti-mouse Atto 647N was used to perform immunohistochemistry in order to show that normal brain development needs microglia-mediated synaptic pruning to the paper

Dianova

sheep-anti-mouse, HRP conjugated antibody was used for Western blotting, in order to demonstrate optogenetics as a useful tool for controlling fertilization and cAMP signaling in sperm to the paper

Dianova anti-mouse coupled to horseradish peroxidase was used in 1:10000 to perform western blot in order to show that in Drosophila centromere formation could be induced by CENH3 to the paper

Santa Cruz Biotechnology

Santa Cruz Biotechnology Horseradish perioxidase conjugated anti-mouse 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 goat anti-mouse HRP secondary antibody was used to perform western blot in order to study the usage of Poly-Ribo-Seq in translating the small open reading frames to the paper

Santa Cruz Biotechnology HRP-conjugated goat anti-mouse 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-mouse 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 goat anti-mouse HRP-conjugated secondary antibody was used to perform western blot in order to investigate the mechanism of self-cleavage of MYRF to the paper

Santa Cruz Biotechnology donkey anti-mouse HRP conjugated antibody was used to perform immunocytochemistry in order to investigate the regulatory effect of TRPM5 activation on MUC5AC secretion from human colon goblet cells to the paper

Santa Cruz HRP-conjugated anti-mouse-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

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

Santa Cruz HRP-labeled anti-mouse 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 HRP conjugated anti-mouse 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

MilliporeSigmaMilliporeSigma anti-mouse IgG H+L secondary antibody product

Horseradish peroxidase-conjugated antibody to mouse 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

HRP conjugated anti-mouse 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

Sigma-Aldrich goat anti-mouse 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 Fc-specific anti-mouse-HRP secondary antibody was used to perform western blot in order to investigate the regulatory role of Erf2 in protein palmitoylation and meiotic entry in Schizosaccharomyces pombe to the paper

Sigma anti-goat and anti-mouse or rabbit IgG peroxidase conjugate antibody was used to carry out western blot assay in order to investigate the regulatory role of Zfp521 in determining the switch between the adipogenic and osteogenic lineages to the paper

Sigma-Aldrich HRP-conjugated goat anti-mouse secondary antibody was used to perform ELISA in order to show that PrP antibody injection could not induce apoptosis in mice hippocampal neurons to the paper

Sigma alkaline phosphatase-conjugated polyclonal goat anti-mouse IgG Fc was used to perform antibody response analysis in order to show that physicochemical damage could activate T helper 2 cell to induce atopic response through NKG2D to the paper

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

Sigma FITC-conjugated goat anti-mouse IgG-Fc was used to perform flow cytometry in order to show that immune activation induced by agonistic CD40 antibodies could be enhanced by inhibitory Fcgamma receptor Fcgamma RIIB engagement to the paper

Sigma HRP-conjugated goat anti-mouse 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

Bio-Rad

Bio-Rad goat anti-mouse HRP was used to perform dot blot in order to investigate the important role of Rad51p in the formation of RNA-DNA hybrids in budding yeast to the paper

Bio-rad secondary goat anti-mouse 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 170-6516 to the paper

goat anti-mouse horseradish peroxidase was used for VSV-G transport assay, in order to study the function of Rab6A binding to KIF1C's motor domain to the paper

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

Bio-Rad anti mouse-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

Bio-Rad HRP-conjugated anti-mouse was used as a secondary antibody in western blot analysis to study the suppression of adipocyte differentiation performed by SIRT2 to the paper

Cell Signaling Technology

Cell signaling anti-mouse 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-mouse IgG was used to perform immunocytochemistry in order to investigate the regulatory effect of HILDA complex on VEGF-A expression to the paper

Cellsignaling mouse anti-biotin-peroxidase antibody was used at 1:2,000 to perform western blot in order to show that the excitability of SCN neurons could be regulated by circadian changes of redox state to the paper

Cell Signaling horseradish peroxidase-labeled mouse secondary antibody was used to assay kinase activity in order to investigate the effect of merlin on glial cell growth to the paper

SouthernBiotech

AP-conjugated goat anti-mouse IgG was used for ELISA, in order to identify the transforming growth factor beta signaling pathway for the generation of Tfh cells and humoral responses during respiratory viral infections to the paper

Southern Biotechnology Associates alkaline phosphatase-conjugated polyclonal goat anti-mouse IgG antibody was used to perform ELISA in order to investigate the relationship between pathogen colonization of the intestine and bacterial virulence to the paper

Southern Biotech HRP conjugated anti-mouse Ig was used to perform ELISA in order to show that at late stages of chronic viral infection interleukin-6 is essential for viral control to the paper

Dako

Dako HRP-conjugated goat anti-mouse antibody was used to perform western blot in order to study the inhibition of signal peptide-binding drugs on the co-translational protein translocation to the paper

Dako anti-Mouse 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 to the paper

DAKO anti-mouse 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-mouse was used to perform western blot in order to show that ciliogenesis was regulated by an evolutionarily assembled cis-regulatory module to the paper

DAKO Goat anti-Mouse-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

DakoCytomotion secondary HRP-conjugated polyclonal goat anti-mouse 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-mouse 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

Diagenode

Diagenode anti-Mouse 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

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-mouse 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-mouse 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-mouse was used to perform western blot in order to study the function of eEF1A1 in transcription during heat shock response to the paper

Amersham Biosciences horseradish peroxidase-conjugated anti-mouse secondary antibody was used to perform western blot in order to study the mechanism of the action potential initiation in neocortical inhibitory interneurons to the paper

Amersham Biosciences sheep anti-mouse diluted in 1:5,000 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

Amersham HRP-conjugated goat anti-mouse IgG was used to perform immunohistochemistry in order to study synaptic plasticity to the paper

GE healthcare anti-mouse 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 HRP-labeled anti-mouse 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 horseradish peroxidase-conjugated anti-mouse IgG 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 ECL sheep anti-mouse-HRP was used at 1:10,000 to perform western blot in order to show the characteristics of piRNAs in Caenorhabditis elegans to the paper

GE Healthcare ECL Mouse IgG, HRP-Linked Whole Ab from sheep 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-mouse secondary antibodies were used to perform western blot in order to show that H-NS could promote chromosome organization in bacteria to the paper

GE Healthcare sheep anti-mouse secondary antibody was used in 1:5,000 to perform western blot in order to show that genomic instability could be induced by aneuploidy in budding yeast to the paper

GE Healthcare horseradish peroxidase-conjugated anti-mouse secondary antibody was used in western blot in order to demonstrate that heparanase can promote expression of syndecan-1 in the nucleus to the paper

Amersham anti-mouse secondary antibody conjugated with peroxidase was used for western blot in order to investigate the role of Cdx activity in the embryo development to the paper

Amersham horseradish peroxidase-conjugated sheep anti-mouse 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

Amersham Bioscience HRP-linked sheep anti-mouse IgG was used to carry out western blot analysis in order to investigate the influence of HCMV infection on expression of MMPs in human macrophages to the paper

LI-COR Biosciences

LI-COR Biosciences goat anti-mouse IgG IRDye 680 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

LI-COR Biosciences IRDye 800CW goat-anti-mouse secondary antibody was used to perform western blotting in order to study the morphogenesis of Stentor to the paper

Li-Cor secondary IRDye 680LT Goat anti-Mouse IgG antibody was used to perform western blot in order to show that MAPK misactivation could be insulated by Ste5 conformational changes to the paper

Licor IRDye800 anti-mouse secondary antibody was used in 1:25,000 to perform western blot in order to show that the detail of yeast meiotic program was revealed by mRNA abundance and protein production measurement to the paper

Li-Cor anti-mouse 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-mouse IRDye800 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 goat anti-mouse IRdye-680CW 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

Vector Laboratories

Vector Labs goat anti-mice 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

BD Biosciences

Becton Dickinson anti-mouse Igk and negative control compensation particles were used to perform flow cytometry in order to show that human long-term engrafting HSCs could be isolated with CD49f as a marker 552843 to the paper

BD Pharmingen PE-conjugated goat anti-mouse IgG antibody was used to perform flow cytometry in order to study the mechanism of immune evasion in cowpox virus to the paper

BD Biosciences anti-mouse IgG-HRP antibody was used to perform ELISA in order to show that commensal bacteria was restricted in specific sites by innate lymphoid cells to the paper

EMD Millipore

Millipore anti-mouse Alexa488 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

Upstate anti-mouse IgG was used to perform ChIP assays in order to illustrate that the Bmi1 functions on neurons oxidative metabolism are associated with repression of p53 pro-oxidant activity to the paper

Boehringer Mannheim

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

Electron Microscopy Sciences

Electron Microscopy Science anti-mouse IgG secondary antibodies conjugated to 10 nm gold particles were used to perform transmission electronic microscopy in order to study the role for PICK1 and ICA69 in regulating the formation and maturation of insulin granules to the paper

Bethyl

Bethyl HRP-conjugated goat anti-mouse IgG was used to perform western blot in order to investigate the regulatory effect of PD-1 on IgA selection and the composition of the gut microflora to the paper

Polysciences

Polysciences goat anti-mouse IgG magnetic beads were used to immunoprecipitate FOXO1-Flag in immunoprecipitation to study FOXO1's interaction with PPAR to study the suppression of adipocyte differentiation performed by SIRT2 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
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
Tsubota T, Okubo Suzuki R, Ohashi Y, Tamura K, Ogata K, Yaguchi M, et al. Cofilin1 controls transcolumnar plasticity in dendritic spines in adult barrel cortex. PLoS Biol. 2015;13:e1002070 pubmed publisher
Binotti B, Pavlos N, Riedel D, Wenzel D, VorbrÃ¼ggen G, Schalk A, et al. The GTPase Rab26 links synaptic vesicles to the autophagy pathway. elife. 2015;4:e05597 pubmed publisher
Overlack K, Primorac I, Vleugel M, Krenn V, Maffini S, Hoffmann I, et al. A molecular basis for the differential roles of Bub1 and BubR1 in the spindle assembly checkpoint. elife. 2015;4:e05269 pubmed publisher
Jansen V, Alvarez L, Balbach M, StrÃ¼nker T, Hegemann P, Kaupp U, et al. Controlling fertilization and cAMP signaling in sperm by optogenetics. elife. 2015;4: pubmed publisher
Madden L, Juhas M, Kraus W, Truskey G, Bursac N. Bioengineered human myobundles mimic clinical responses of skeletal muscle to drugs. elife. 2015;4:e04885 pubmed publisher
Marshall H, Ray J, Laidlaw B, Zhang N, Gawande D, Staron M, et al. The transforming growth factor beta signaling pathway is critical for the formation of CD4 T follicular helper cells and isotype-switched antibody responses in the lung mucosa. elife. 2015;4:e04851 pubmed publisher
Rebello M, McTavish T, Willhite D, Short S, Shepherd G, Verhagen J. Perception of odors linked to precise timing in the olfactory system. PLoS Biol. 2014;12:e1002021 pubmed publisher
Vermeire K, Bell T, Van Puyenbroeck V, Giraut A, Noppen S, Liekens S, et al. Signal peptide-binding drug as a selective inhibitor of co-translational protein translocation. PLoS Biol. 2014;12:e1002011 pubmed publisher
Doherty J, Sheehan A, Bradshaw R, Fox A, Lu T, Freeman M. PI3K signaling and Stat92E converge to modulate glial responsiveness to axonal injury. PLoS Biol. 2014;12:e1001985 pubmed publisher
Modell J, Kambara T, Perchuk B, Laub M. A DNA damage-induced, SOS-independent checkpoint regulates cell division in Caulobacter crescentus. PLoS Biol. 2014;12:e1001977 pubmed publisher
Oh Y, Yoon S, Zhang Q, Chae H, DaubnerovÃ¡ I, Shafer O, et al. A homeostatic sleep-stabilizing pathway in Drosophila composed of the sex peptide receptor and its ligand, the myoinhibitory peptide. PLoS Biol. 2014;12:e1001974 pubmed publisher
Lahiri S, Chao J, Tavassoli S, Wong A, Choudhary V, Young B, et al. A conserved endoplasmic reticulum membrane protein complex (EMC) facilitates phospholipid transfer from the ER to mitochondria. PLoS Biol. 2014;12:e1001969 pubmed publisher
Schroeder C, Ostrem J, Hertz N, Vale R. A Ras-like domain in the light intermediate chain bridges the dynein motor to a cargo-binding region. elife. 2014;3:e03351 pubmed publisher
Botelho J, Ossa Fuentes L, Soto Acuña S, Smith Paredes D, Núñez León D, Salinas Saavedra M, et al. New developmental evidence clarifies the evolution of wrist bones in the dinosaur-bird transition. PLoS Biol. 2014;12:e1001957 pubmed publisher
Lebon L, Lee T, Sprinzak D, Jafar Nejad H, Elowitz M. Fringe proteins modulate Notch-ligand cis and trans interactions to specify signaling states. elife. 2014;3:e02950 pubmed publisher
Tata B, Huijbregts L, Jacquier S, Csaba Z, Genin E, Meyer V, et al. Haploinsufficiency of Dmxl2, encoding a synaptic protein, causes infertility associated with a loss of GnRH neurons in mouse. PLoS Biol. 2014;12:e1001952 pubmed publisher
Schueren F, Lingner T, George R, Hofhuis J, Dickel C, Gartner J, et al. Peroxisomal lactate dehydrogenase is generated by translational readthrough in mammals. elife. 2014;3:e03640 pubmed publisher
Vera M, Pani B, Griffiths L, Muchardt C, Abbott C, Singer R, et al. The translation elongation factor eEF1A1 couples transcription to translation during heat shock response. elife. 2014;3:e03164 pubmed publisher
Günesdogan U, Jackle H, Herzig A. Histone supply regulates S phase timing and cell cycle progression. elife. 2014;3:e02443 pubmed publisher
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