This is a Validated Antibody Database (VAD) review about anti-goat secondary antibody, based on 43 published articles (read how Labome selects the articles), using anti-goat secondary antibody product in experiments. It is aimed to help Labome visitors find the most suited anti-goat secondary antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
Molecular Probes Alexa Fluor 488 rabbit anti-goat IgG was used to perform immunocytochemistry in order to show the role of cell adhesion and cortex tension in cell sorting during gastrulation A-11078to the paper
Invitrogen Alexa 647-conjugated donkey anti-goat was used to perform immunohistochemistry in order to study the mechanism of the action potential initiation in neocortical inhibitory interneurons to the paper
Life Technologies anti-goat-raised Alexa Fluor 568 antibody was used to perform immunoflurescene to study the modulatory effect of gephyrin on GABAergic synapses to the paper
Molecular probes donkey anti-goat Alexa 647 was used to perform immunofluorescence in order to study Nodal expression regulates differentiation of epiblast cells to the paper
Molecular Probes Cy3-donkey anti-goat antibody was used to perform immunohistochemistry in order to investigate the role of CDON in regulating tumor cell survival to the paper
Invitrogen Alexa Fluor 488 (Fab')2 fragment of rabbit anti-goat IgG (H+L) was used to perform immunohistochemistry in order to investigate the mechanism of tip link regeneration in auditory hair cells to the paper
Invitrogen donkey-anti-goat-Alexa-Fluor 546 was used to perform immunohistochemistry 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
Invitrogen normal goat IgG was used to perform whole mount staining in order to show that specific myeloid cells derived from the yolk sac to the paper
Invitrogen anti-goat Alexa Fluor 555 was used in 1:500 to perform immunohistochemistry in order to show that proper organogenesis needs B-type lamins in mice to the paper
Invitrogen Alexa Fluor 555-conjugated donkey anti-goat IgG was used to perform immunocytochemistry in order to show that Legionella gets amino acids for growth by promoting eukaryotic proteasomal degradation to the paper
Invitrogen Alexa488-labeled donkey anti-goat IgG was used in 1:300 to perform immunocytochemistry in order to show that axonal projection could be regulated by cartilage acidic protein-1B through NgR1 inhibition to the paper
Invitrogen Alexa Fluor 546 donkey anti-goat antibody was used as secondary antibody to wash and incubate the sections in order to determine the ATM expression patterns and studied its localization to the paper
Molecular Probes donkey anti-goat AlexaFluor 680-labeled antibody was used to perform westernblot in order to locate KCNE1 relative to KCNQ1 in the potassium channel to the paper
Invitrogen rabbit anti-goat IgG (H+L) FITC conjugate was used to quantify surface HLA-C molecule expression in order to identify the MHC I molecule (HLA-C) as an attachment factor in facilitating HCoV-HKU1 spike (S) mediated infection to the paper
Jackson ImmunoResearch Laboratories
Jackson ImmunoResearch donkey anti-goat-Alexa488 was used to perform immunohistochemistry in order to investigate the roles of VAL- and TMT-opsins in neuronal photoreception in medaka fish and zebrafish 705-545-147to the paper
Dylight-649 labeled anti-goat 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
Jackson Immunoresearch biotin-conjugated donkey anti-goat IgGs were used to perform immunohistochemistry in order to study brain endothelial cells control reproduction through Semma3A-Nrp1 signaling to the paper
Jackson ImmunoResearch Cy5-donkey anti-goat antibody was used to perform immunohistochemistry in order to investigate the role of CDON in regulating tumor cell survival to the paper
Jackson ImmunoResearch goat isotype IgG was used to perform blocking in order to investigate the role of sFLT-1 in the maintenance of the avascular photoreceptor layer in mouse models to the paper
Jackson Immunoresearch biotinylated anti-goat antibody was used to perform flow cytometry in order to investigate the important role of EBI2 in CD4+ dendritic cell positioning, homeostasis and blood-borne particulate antigen capture to the paper
Jackson ImmunoResearch HRP-conjugated donkey anti-goat 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 anti-goat IgG HRP was used to perform western blot in order to show that proper organogenesis needs B-type lamins in mice to the paper
Jackson peroxidase-conjugated rabbit-anti-goat H+L was used in 1:1000 to perform ELISA in order to show that HIV glycan coat could be recognized by PGT antibody to neutralize HIV to the paper
Jackson ImmunoResearch Laboratories HRP-conjugated donkey anti-goat IgG secondary antibody was used in western blot in order to study the role of IgSF8 and CD9 in mammalian sperm-egg interaction to the paper
Jackson ImmunoResearch donkey anti-goat Ig-HRP antibody was used in western blot to treat mice in order to confirm that Bcl-3 is part of the pathway whereby adjuvants affect T cell lifespans to the paper
Rockland anti-goat 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
R&D Systems goat IgG was used to perform cell culture in order to investigate the role of PVRL4 in tumor progression to the paper
Abcam biotinylated secondary donkey anti-goat antibody was used to perform immunohistochemistry in order to show that NKT cells could be modulated by exposure to microbes during early life to the paper
Santa Cruz Biotechnology
Santa Cruz Biotechnology Horseradish perioxidase conjugated anti-goat 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 donkey anti-goat 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 Biotechnology rhodamine-conjugated donkey anti-goat IgG was used to perform immunocytochemistry in order to investigate the mechanism of self-cleavage of MYRF to the paper
Santa Cruz Biotechnology donkey anti-goat 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
Santa Cruz goat-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 Biotech PE-anti-goat secondary antibody was used to perform immunocytochemistry in order to show that antigen presentation capacity is affected by asymmetric segregation of polarized antigen on B cell division to the paper
Santa Cruz HRP-labeled anti-goat 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 donkey anti-goat antibody coupled to horseradish peroxidase was used in 1:10,000 to perform western blot in order to show that genomic instability could be induced by aneuploidy in budding yeast to the paper
SantaCruz Biotechnology HRP-conjugated rabbit anti-goat secondary antibody was used to incubate the membranes in order to study that the hoxd4 gene represses its expression at the transcriptional level in human breast cancer cells to the paper
Santa Cruz Biotechnology anti-goat peroxidase conjugate secondary antibody was used to process the samples for immunoblotting in order to indicate that SUMOylation is mediated through reduced CDK7-induced phosphorylation of SF-1 to the paper
MilliporeSigma
HRP conjugated anti-goat 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
Dako
Dako anti-Goat 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 rabbit anti-Goat-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-goat 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
Cell Signaling Technology
Cell signaling anti-goat secondary antibody was used to perform western blotting in order to study type III interferon (IFN) suppresses tumor growh to the paper
Vector Laboratories
Vector Labs biotinylated anti-mouse or anti-goat IgG was used in 1:2000 to perform immunohistochemistry in order to show that cell fate choice could be modulated by chromatin "prepattern" and histone modifiers to the paper
BD Biosciences
BD Biosciences PE-labeled rabbit anti-goat 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
BBI Solutions
BB International Immuno-gold Conjugate EM rabbit anti-goat 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
Articles Reviewed
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  29. Price C, Al Quadan T, Santic M, Rosenshine I, Abu Kwaik Y. Host proteasomal degradation generates amino acids essential for intracellular bacterial growth. Science. 2011;334:1553-7 pubmed publisher
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  32. Janssen A, van der Burg M, Szuhai K, Kops G, Medema R. Chromosome segregation errors as a cause of DNA damage and structural chromosome aberrations. Science. 2011;333:1895-8 pubmed publisher
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