
Thermo Fisher Scientific CD59 Monoclonal Antibody (1F5)
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Applications
Tested Dilution
Publications
Flow Cytometry (Flow)
1 µg/1 million 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 = \[{
targetFamily:
CD59,
uniProtId:
P13987-1,
ncbiNodeId:
9606,
antigenRange:
1-128,
antigenLength:
128,
antigenImageFileName:
MA1-70058_CD59_P13987-1_House_mouse.svg,
antigenImageFileNamePDP:
MA1-70058_CD59_P13987-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
View additional formats
Form
Liquid
Concentration
1 mg/mL
Purification
Protein G
Storage buffer
PBS
Contains
0.02% sodium azide
Storage conditions
4° C
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_1073175
Product Specific Information
MA1-70058 detects CD59 in human samples.
MA1-70058 has been successfully used in flow cytometry procedures.
The MA1-70058 immunogen is Neuraminidase-treated Human Erythrocytes (Neu-HuE).
Store at 4ºC. For long term storage, alilquot and freeze unused portion at -20ºC in single use volumes. Avoid freeze/thaw cycles.
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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