Anti-Rat CD4 (Clone OX-38) – Purified in vivo GOLD™ Functional Grade
Anti-Rat CD4 (Clone OX-38) – Purified in vivo GOLD™ Functional Grade
Product No.: C752
Clone OX-38 Target CD4 Formats AvailableView All Product Type Hybridoma Monoclonal Antibody Alternate Names T-cell surface glycoprotein CD4, T-cell surface antigen T4/Leu-3, W3/25
antigen Isotype Mouse IgG2a Applications Depletion , ELISA , FA , FC , IP |
Antibody DetailsProduct DetailsReactive Species Rat Host Species Mouse Recommended Dilution Buffer Immunogen Lymphocytes or thymocyte glycoproteins Product Concentration ≥ 5.0 mg/ml Endotoxin Level < 1.0 EU/mg as determined by the LAL method Purity ≥95% monomer by analytical SEC ⋅ >95% by SDS Page Formulation This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration. State of Matter Liquid Product Preparation Functional grade preclinical antibodies are manufactured in an animal free facility using only in vitro protein free cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates. Storage and Handling Functional grade preclinical antibodies may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ -70°C. Avoid Repeated Freeze Thaw Cycles. Regulatory Status Research Use Only Country of Origin USA Shipping 2 – 8° C Wet Ice Additional Applications Reported In Literature ? Depletion, ELISA, FA, FC, IP Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity OX-38 activity is directed against rat CD4. Background CD4 is a 55 kD single-chain type I transmembrane glycoprotein with four domains and is a
member of the Ig superfamily1,2. CD4 functions primarily as a coreceptor for the MHC class II
molecule-peptide complex and initiates the early phase of T-cell activation via its association
with the T-cell receptor complex and protein tyrosine kinase Lck3. In addition, CD4 T
lymphocytes are essential to the host response against infectious disease4 and CD4 T cells
mediate neuronal damage in infectious and immune-mediated diseases of the central nervous
system5. In macrophages and natural killer cells, CD4 plays a role in differentiation/activation,
cytokine expression and cell migration3. OX-38 was generated by immunizing mice with lymphocytes or thymocyte glycoproteins and subsequently fusing mouse spleen cells with the P3-X63/Ag 8 cell line6. OX-38 is a depleting monoclonal antibody used to study tolerance to allografts7,8,9,10,11 , Pneumocystis-host interaction4, and alopecia12 in rat models. Antigen Distribution CD4 is expressed on most thymocytes, a subset of T cells, and on
monocytes/macrophages. Ligand/Receptor LCK, PTK2/FAK1, P4HB/PDI, IL16, MHCII alpha and beta chains NCBI Gene Bank ID UniProt.org Research Area Adaptive Immunity . Immunology . Autoimmunity Leinco Antibody AdvisorPowered by AI: AI is experimental and still learning how to provide the best assistance. It may occasionally generate incorrect or incomplete responses. Please do not rely solely on its recommendations when making purchasing decisions or designing experiments. In Vivo Applications of Clone OX-38 in MiceOverview In Vivo Functions in Rats (Not Mice)
Clarification for Mouse StudiesOX-38 is not reactive with mouse CD4; it is specific to rat CD4. For in vivo CD4+ T cell depletion or modulation in mice, researchers use antibodies such as YTS 177 or GK1.5, which are specific to mouse CD4. There is no evidence in the provided search results that OX-38 is used in mouse in vivo studies. Technical Details
ConclusionClone OX-38 is extensively used in rats for in vivo depletion and functional modulation of CD4+ T cells, but it is not applicable for similar purposes in mice due to species specificity. For mouse studies, alternative anti-CD4 clones (e.g., YTS 177, GK1.5) must be used. Based on the available search results, there is limited specific information about antibodies commonly used alongside OX-38. However, some relevant associations can be identified from the literature. Related CD4 AntibodiesThe W3/25 monoclonal antibody is closely related to OX-38, as both antibodies recognize the same or adjacent epitopes on the rat CD4 antigen. These two antibodies are often discussed together in the literature because they bind to Domain 1 of CD4, though they differ in their functional properties. Notably, W3/25 is characterized as a nondepleting antibody, whereas OX-38 functions as a CD4+ T-cell-depleting antibody. This distinction makes them useful for comparative studies examining different approaches to modulating CD4+ T cell function. The OX-35 monoclonal antibody represents another anti-rat CD4 antibody, though it recognizes a different epitope than both OX-38 and W3/25. This makes OX-35 potentially useful as a complementary tool for studying different domains or functional aspects of the CD4 molecule. Limited Information AvailableThe search results primarily focus on characterizing OX-38 itself rather than describing experimental systems where it is used in combination with other antibodies or proteins. While the results mention that OX-38 is used in various applications including flow cytometry, immunohistochemistry, and in vivo depletion studies, they do not provide comprehensive information about which other antibodies or proteins are routinely paired with it in published research. To obtain more detailed information about commonly co-used reagents with OX-38 in specific experimental contexts, a more targeted literature search focusing on published research articles utilizing this antibody would be necessary. In scientific literature, clone OX-38 is primarily associated with antibodies targeting rat CD4, a surface glycoprotein on T cells. Here are the key findings related to OX-38:
While direct citations specifically discussing key findings from OX-38 in broader scientific contexts are not extensively detailed in the search results, the clone is a valuable tool in immunology research, particularly in studies involving rat models. Dosing regimens of OX-38 (an anti-rat CD4 monoclonal antibody, commonly used for CD4 T cell depletion in mice) are not provided directly in the search results. However, relevant published protocols and dosing regimens for similar depleting antibodies against CD4 (like GK1.5, YTS191.1) can be inferred, but specifics for OX-38 itself are missing from the results returned. Here is an evidence-based summary:
Summary table (regimen for typical CD4-depleting mAbs in mice, generalizable to OX-38):
Direct data for OX-38-specific dosing for different mouse models is not present in the search results, so the answer reflects expert standard practice for in vivo CD4-depletion derived from antibody dosing guides and immunogenicity modeling in mouse protocols. References & Citations1. Lynch GW, Turville S, Carter B, et al. Immunol Cell Biol. 84(2):154-165. 2006. 2. Wittlich M, Thiagarajan P, Koenig BW, et al. Biochim Biophys Acta. 1798(2):122-127. 2010. 3. https://www.uniprot.org/uniprotkb/P05540/entry 4. Thullen TD, Ashbaugh AD, Daly KR, et al. Infect Immun. 71(11):6292-6297. 2003. 5. Brunn A, Utermöhlen O, Carstov M, et al. Am J Pathol. 173(1):93-105. 2008. 6. Jefferies WA, Green JR, Williams AF. J Exp Med. 162(1):117-127. 1985. 7. Flavin T, Shizuru J, Seydel K, et al. J Heart Transplant. 9(5):482-488. 1990. 8. Arima T, Lehmann M, Flye MW. Transplantation. 63(2):284-292. 1997. 9. Motoyama K, Arima T, Lehmann M, et al. Surgery. 122(2):213-219. 1997. 10. Qi Z, Riesbeck K, Ostraat O, et al. Transpl Immunol. 5(3):204-211. 1997. 11. Shizuru JA, Seydel KB, Flavin TF, et al. Transplantation. 50(3):366-373. 1990. 12. McElwee KJ, Spiers EM, Oliver RF. Br J Dermatol. 140(3):432-437. 1999. Technical ProtocolsCertificate of Analysis |
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