This is a Validated Antibody Database (VAD) review about anti-rat IgG H+L secondary antibody, based on 56 published articles (read how Labome selects the articles), using anti-rat IgG H+L secondary antibody product in experiments. It is aimed to help Labome visitors find the most suited anti-rat 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 APC-labeled donkey anti-rat 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
Molecular Probes Alexa Fluor 546 goat anti-rat IgG was used to perform immunocytochemistry in order to show the role of cell adhesion and cortex tension in cell sorting during gastrulation A-11081to the paper
Alexa 568-conjugated donkey anti-rat IgG was used in immunohistochemical assay in order to study the role of intracellular polarity in myelination and remyelination to the paper
Invitrogen goat anti-rat 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 goat anti-rat IgG conjugated to Alexa555 was used to perform immunohistochemistry in order to study the developmental relationship between mesenchymal stem cells with hematopoietic stem cells to the paper
Invitrogen Alexa Fluor 488-conjucated anti-rat 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
Molecular Probes alexa's 488 conjugated anti-rat 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
Thermo Scientific horse radish peroxidase (HRP)-conjugated goat anti-rat secondary antibody was used to perform western blot in order to show that MID gene is critical for sperm and egg development in V. carteri to the paper
Life Technologies anti-rat Alexa488 was used as a secondary antibody in order to perform immunofluorescence assay of the changes in the localization of the proteins fused with HA tag to the paper
Invitrogen anti-rat secondary antibody was used to perform immunohistochemistry in order to study the mechanism of cell elongation to the paper
Invitrogen anti-rat IgG secondary antibody was used to perform immunohistochemistry in order to study synaptic plasticity to the paper
Molecular Probes goat anti-rat 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
Molecular Probes goat anti-rat Alexa647 was used to perform immunohistochemistry in order to study the role of Smurf proteins in controlling Hh signaling to the paper
Life Technologies Alexa-488 anti-rat 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
Invitrogen anti-rat-Cy5 secondary antibody was used to perform immunofluorescence in order to study the contributions of mast cells to dengue virus-induced vascular leakage to the paper
Molecular Probes Alexa 647-conjugated goat anti-rat antibody was used to carry out immunofluorescence assays in order to determine the role of CULLIN-3 in the control of TIM oscillations in the Drosophila circadian clock to the paper
Invitrogen goat anti-rat antibodies were used to perform immunohistochemistry in order to show that skin microbiota could provide protective immunity to the paper
Invitrogen normal rat 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 goat anti-rat 555 was used to perform immunocytochemistry in order to show that physicochemical damage could activate T helper 2 cell to induce atopic response through NKG2D to the paper
Molecular Probes anti-rat Alexa-568 was used in 1:800 to perform immunocytochemistry in order to show that mitochondria and other organelles from sperm are eliminated after fertilization to the paper
Molecular Probes goat anti-rat Alexa Fluor 647 was used to perform immunocytochemistry in order to show that hypoglycemia in humans could be caused by activating mutant AKT2 to the paper
Invitrogen Fluor-594-conjugated goat anti-rat IgM was used to perform immunocytochemistry in order to show that sialyl-Lewis(x) oligosaccharide on the zona pellucida is responsible for sperm-oocyte binding to the paper
Invitrogen anti-rat IgG horseradish peroxidase conjugate was used in 1:2500 to perform ELISA in order to show the structural basis of RON2 peptide interaction with AMA1 for apicomplexan parasite invasion to the paper
Invitrogen Alexa Fluor 488 anti-rat IgG was used to perform flow cytometry in order to show that DNA methylation of Rasgrf1 locus was modulated by piRNAs and noncoding RNA to the paper
Molecular Probes Cy3-conjugated anti-rat 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
Molecular Probes Alexa Fluor 488 goat anti-rat IgG was used to perform immunofluorescence in order to reveal VZV IE63 protein interacts with human ASF1 protein and increases the binding of ASF1 to histone H3.1 and H3.3 to the paper
Dynal Biotech sheep anti-rat Dynabeads were used in cell depletion to identify a clonogenic bone marrow progenitor specific for macrophages and dendritic cells to the paper
Jackson ImmunoResearch LaboratoriesJackson ImmunoResearch Laboratories anti-rat IgG H+L secondary antibody product
Jackson ImmunoResearch Cy3 anti-rat IgG was used to perform immunohistochemistry in order to study the mechansim of the glial responsiveness to axonal injury in Drosophila to the paper
Jacksons Immunoresearch Cy5-conjugated donkey anti rat 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 alkaline phosphatase-conjugated anti-rat 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 Immuno Research rat IgG 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 Immuno Research Laboratories goat anti-rat-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
Jackson ImmunoResearch Cy5 goat anti-rat 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 ImmunoResearch Rhodamine Red-X-conjugated donkey anti-rat 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 ImmunoResearch Cy5-conjugated donkey-anti-rat 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 Cy3-conjugated goat anti-rat 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 Cy5-donkey-anti-rat IgG was used to perform immunohistochemistry in order to show that PAH metabolism mediated by Langerhans cells leads to DNA damage and tumorigenesis to the paper
Jackson Immunoresearch anti-rat FITC antibody was used in 1:100 to perform immunocytochemistry in order to show that the detail of yeast meiotic program was revealed by mRNA abundance and protein production measurement to the paper
Jackson ImmunoResearch Laboratories rabbit anti-Rat Cy2 antibody was used to perform immunocytochemistry in order to show that lysosome function and macrophage homeostasis were disrupted without ENT3 to the paper
Jackson ImmunoResearch biotinylated donkey anti-rat Ig was used to perform immunohistochemistry in order to show that the formation of intestinal lymphoid follicles needs AhR activation by dietary ligands to the paper
Jackson ImmunoReaserch donkey anti-rat IgG biotin was used to perform flow cytometry in order to show that migration of lymphocytes from blood to lymphoid tissues needs GRK2-dependent S1PR1 desensitization to the paper
Jackson Immunoresearch anti-rat PE secondary antibody was used to perform flow cytometry in order to show that at late stages of chronic viral infection interleukin-6 is essential for viral control to the paper
Jackson Immunoresearch anti-rat FITC was used at a 1:100 dilution to perform immunocytochemistry in order to show that genomic instability could be induced by aneuploidy in budding yeast to the paper
Jackson ImmunoResearch anti-rat IgG-Cy3 was used in 1:250 to perform immunohistochemistry in order to show that LR asymmetric tissue morphogenesis is determined by planar cell-shape chirality to the paper
Jackson ImmunoResearch rhodamine-conjugated goat-anti-rat antibody was used to carry out immunofluorescence assays in order to investigate the mechanism for CEA-binding bacteria counteracting shedding of epithelial cells to the paper
Jackson Laboratories fluorscence-conjugated anti-rat antibody was used to perform immunocytochemistry in order to study the mechanism by which Drosophila microRNAs 263a/b confer robustness during development to the paper
Jackson anti-rat IgG peroxidase-conjugated antibody was used to detect immunoprecipitated cloned KSHV ORF proteins in Western blot as a secondary antibody to the paper
Jackson Immunoresearch Cy3-conjugated goat anti-rat IgG antibody was used in immunohistochemistry to identify a clonogenic bone marrow progenitor specific for macrophages and dendritic cells to the paper
BioLegend
Biolegend goat anti-rat IgG- phycoerythrin (PE) antibody was used to perform flow cytometry in order to show that cell fate choice could be modulated by chromatin "prepattern" and histone modifiers to the paper
Miltenyi Biotec
Miltenyi bead-coupled goat anti-rat secondary antibodies were used to perform cell isolation in order to show that fetomaternal immune tolerance was regulated by chemokine gene silence in decidual stromal cells to the paper
Santa Cruz Biotechnology
Santa Cruz Biotechnology HRP-conjugated goat anti-rat 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 HRP-conjugated goat anti-rat 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
Boster
Boster BioTec HRP-goat anti-rat IgG antibody 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
Dianova
goat-anti-rat, 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
MilliporeSigma
Sigma-Aldrich anti-rat IgG-FITC 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 F6258to the paper
Sigma TRITC-labeled rat IgG was used to perform immunohistochemistry in order to show that axonal projection could be regulated by cartilage acidic protein-1B through NgR1 inhibition to the paper
Dako
DakoCytomation biotin-conjugated anti-rat 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
LI-COR Biosciences
Li-Cor anti-rat 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
Vector Laboratories
Vector Labs biotinylated rabbit anti-rat secondary antibody was used in 1:500 to perform immunohistochemistry in order to show that mammals may have cardiac regeneration ability for a brief period after birth to the paper
donkey anti-rat Alexa488 antibody was used for immunohistochemistry, in order to demonstrate optogenetics as a useful tool for controlling fertilization and cAMP signaling in sperm to the paper
Kirkegaard & Perry Laboratories
Kirkegaard and Perry Laboratories goat anti-rat IgG conjugated to horseradish peroxidase was used to perform ELISA in order to study the role for surfactant protein A in protecting the immunocompetent host from exposure to Pneumocystis colonization to the paper
Qiagen
Qiagen Goat anti-Rat IgG beads were used to obtain lineage-negative BM cells in order to study the mechanism of the Lmo2 oncogene induced mice leukemia to the paper
Articles Reviewed
- Hu X, Feng F, Wang Y, Wang L, He F, Dou G, et al. Blockade of Notch signaling in tumor-bearing mice may lead to tumor regression, progression, or metastasis, depending on tumor cell types. Neoplasia. 2009;11:32-8 pubmed
- Fukata Y, Adesnik H, Iwanaga T, Bredt D, Nicoll R, Fukata M. Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission. Science. 2006;313:1792-5 pubmed
- Fogg D, Sibon C, Miled C, Jung S, Aucouturier P, Littman D, et al. A clonogenic bone marrow progenitor specific for macrophages and dendritic cells. Science. 2006;311:83-7 pubmed
other review
questions and comments