
Thermo Fisher Scientific CD59/Complement Regulatory Protein/Protectin Monoclonal Antibody (193-27)
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Applications
Tested Dilution
Publications
Immunohistochemistry (Paraffin) (IHC (P))
Assay-dependent
Immunocytochemistry (ICC/IF)
1-2 µg/mL
Flow Cytometry (Flow)
1-2 µg/10^6 cells
Functional Assay (Functional)
Assay-dependent
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgM, kappa
Class
Monoclonal
Type
Antibody
Clone
193-27
Immunogen
Stimulated human leukocytes if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
CD59,
uniProtId:
P13987-1,
ncbiNodeId:
9606,
antigenRange:
1-128,
antigenLength:
128,
antigenImageFileName:
966-MSM1-P0_CD59_P13987-1_House_mouse.svg,
antigenImageFileNamePDP:
966-MSM1-P0_CD59_P13987-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
200 µg/mL
Purification
Protein A/G
Storage buffer
PBS, pH 7.4, with 0.05% BSA
Contains
0.05% sodium azide
Storage conditions
4° C, do not freeze
Shipping conditions
Ambient (domestic); Wet ice (international)
Product Specific Information
Does not react with Baboon or Horse
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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