Key features and details
- APC Mouse monoclonal [MEM-43] to CD59
- Suitable for: Flow Cyt
- Reacts with: Human
- Conjugation: APC. Ex: 645nm, Em: 660nm
- Isotype: IgG2a
Product nameAPC Anti-CD59 antibody [MEM-43]
See all CD59 primary antibodies
DescriptionAPC Mouse monoclonal [MEM-43] to CD59
ConjugationAPC. Ex: 645nm, Em: 660nm
Specificityab36467 recognises CD59 antigen.
Tested applicationsSuitable for: Flow Cytmore details
Species reactivityReacts with: Human
Human thymocytes and T lymphocytes
EpitopeReacts with the well defined epitope (W40, R-53) on CD59 molecule
- Human whole blood
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Storage instructionsShipped at 4°C. Store at +4°C.
Storage bufferpH: 7.4
Preservative: 0.097% Sodium azide
Constituent: 0.2% BSA
High grade protease free BSA
Concentration information loading...
Purification notesPurified antibody was conjugated with cross-linked APC under optimum conditions. The conjugate was purified by size-exclusion chromatography and adjusted for direct use.
Our Abpromise guarantee covers the use of ab36467 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
FunctionPotent inhibitor of the complement membrane attack complex (MAC) action. Acts by binding to the C8 and/or C9 complements of the assembling MAC, thereby preventing incorporation of the multiple copies of C9 required for complete formation of the osmolytic pore. This inhibitor appears to be species-specific. Involved in signal transduction for T-cell activation complexed to a protein tyrosine kinase.
The soluble form from urine retains its specific complement binding activity, but exhibits greatly reduced ability to inhibit MAC assembly on cell membranes.
Involvement in diseaseDefects in CD59 are the cause of CD59 deficiency (CD59D) [MIM:612300].
Sequence similaritiesContains 1 UPAR/Ly6 domain.
modificationsN- and O-glycosylated. The N-glycosylation mainly consists of a family of biantennary complex-type structures with and without lactosamine extensions and outer arm fucose residues. Also significant amounts of triantennary complexes (22%). Variable sialylation also present in the Asn-43 oligosaccharide. The predominant O-glycans are mono-sialylated forms of the disaccharide, Gal-beta-1,3GalNAc, and their sites of attachment are probably on Thr-76 and Thr-77. The GPI-anchor of soluble urinary CD59 has no inositol-associated phospholipid, but is composed of seven different GPI-anchor variants of one or more monosaccharide units. Major variants contain sialic acid, mannose and glucosamine Sialic acid linked to an N-acetylhexosamine-galactose arm is present in two variants.
Glycated. Glycation is found in diabetic subjects, but only at minimal levels in nondiabetic subjects. Glycated CD59 lacks MAC-inhibitory function and confers to vascular complications of diabetes.
Cellular localizationCell membrane. Secreted. Soluble form found in a number of tissues.
- Information by UniProt
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ab36467 has been referenced in 1 publication.
- Henn AD et al. Functionally Distinct Subpopulations of CpG-Activated Memory B Cells. Sci Rep 2:345 (2012). Flow Cyt ; Human . PubMed: 22468229