
Thermo Fisher Scientific CD59 Monoclonal Antibody (1F5), FITC
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Applications
Tested Dilution
Publications
Flow Cytometry (Flow)
1.0 µg/1x10^6 cells
Product Specifications
Species Reactivity
Human, Mouse
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
1F5
Immunogen
Neuraminidase-treated Human Erythrocytes (Neu-HuE) if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
CD59,
uniProtId:
P13987-1,
ncbiNodeId:
9606,
antigenRange:
1-128,
antigenLength:
128,
antigenImageFileName:
MA5-17738_CD59_P13987-1_House_mouse.svg,
antigenImageFileNamePDP:
MA5-17738_CD59_P13987-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $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
0.1 mg/mL
Purification
Protein G
Storage buffer
PBS with 4-5mg/mL BSA
Contains
0.02% sodium azide
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. Store in the dark.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2539128
Product Specific Information
MA5-17738 targets CD59/Protectin in FACS applications and shows reactivity with Human samples.
The MA5-17738 immunogen is mouse pre-B tumour cells (RAW112).
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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