Anti-CD1 antibody [76-7-4] (ab24986)
- Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
- Storage bufferPreservative: None
Constituents: 100mM Borate buffered saline, pH 8.2
- Concentration information loading...
- PurityIgG fraction
- Clonality Monoclonal
- Clone number76-7-4
- Light chain typekappa
- Research Areas
Our Abpromise guarantee covers the use of ab24986 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-Fr (acetone fixed): Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
- RelevanceAll CD1 molecules, except CD1e, are cell surface glycoproteins that are structurally related to the MHC molecules, however, in distinction, CD1 proteins are essentially non polymorphic. CD1 has considerable structural homology with both MHC class I and class II molecules, and CD1 molecules are involved in T cell activation. In contrast to MHC, however, CD1 molecules appear to present predominantly non peptide molecules originating from lipids and glycolipids.
- Cellular localizationCell Membrane. Type I membrane protein.
- A1 domain antibodyCD1A antibodyCD1A antigen antibody
- CD1B antibodyCD1b antigen antibodyCD1b molecule antibodyCD1C antibodyCD1C antigen antibodyCD1c molecule antibodyCD1D antibodyCD1d molecule antibodyCd1d1 antibodyCortical thymocyte antigen CD1A antibodyCortical thymocyte antigen CD1B antibodyCortical thymocyte antigen CD1C antibodyCortical thymocyte antigen CD1D antibodyhTa1 thymocyte antigen antibodyLy38 antibodyT cell surface glycoprotein CD1a antibodyT cell surface glycoprotein CD1b antibodyT cell surface glycoprotein CD1c antibodyT cell surface glycoprotein CD1d antibodyT6/Leu6 antibody
References for Anti-CD1 antibody [76-7-4] (ab24986)
ab24986 has not yet been referenced specifically in any publications.