
Thermo Fisher Scientific CD59 Monoclonal Antibody (7A6), FITC
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:50
Immunohistochemistry (Frozen) (IHC (F))
1:50
Immunocytochemistry (ICC/IF)
1:50
Flow Cytometry (Flow)
1:50
Functional Assay (Functional)
1:50
Inhibition Assays (IA)
1:50
Product Specifications
Species Reactivity
Mouse
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
7A6
Immunogen
mCD59a-Fc if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
CD59,
uniProtId:
O55186-1,
ncbiNodeId:
10090,
antigenRange:
1-123,
antigenLength:
123,
antigenImageFileName:
MA5-49021_CD59_O55186-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-49021_CD59_O55186-1_House_mouse_PDP.jpeg,
sortOrder:
2}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
FITC FITC FITC
View additional formats
Excitation/Emission Max
498/517 nm View spectra
Form
Liquid
Concentration
100 µg/mL
Purification
Protein G
Storage buffer
PBS with 1% BSA
Contains
0.02% sodium azide
Storage conditions
4° C, store in dark
Shipping conditions
Wet ice
RRID
AB_3093973
Target Information
CD59 (Protectin) is a small (18-20 kDa) GPI-anchored ubiquitously expressed inhibitor of the membrane attack complex (MAC). CD59 is the key regulator that preserves the autologous cells from terminal effector mechanism of the complement cascade. CD59 also associates with C5b-8 complex and counteracts appropriate formation of cytolytic pore within the plasma membrane. Further, CD59 is a low-affinity ligand of human CD2, causes T cell costimulation, and is involved in lymphocyte signal transduction. CD59 is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. Mutations in this gene cause CD59 deficiency, a disease involving hemolytic anemia, thrombosis, and cerebral infarction. Multiple alternatively spliced transcript variants of CD59 have been identified.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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