XIAP antibody

Synonyms:API3 antibody, BIRC4 antibody, hIAP 3 antibody, hIAP3 antibody, hILP antibody, IAP 3 antibody, IAP like protein antibody, IAP3 antibody, ILP antibody, ILP1 antibody, MIHA antibody, X linked IAP antibody, XIAP antibody, XLP2 antibody
Catalogue No.:FNab09540Reactivity:Human, Mouse, Rat
Host:RabbitTested Application:ELISA, WB, IHC, IF
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
XIAP antibody
Catalogue No.
FNab09540
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
X-linked inhibitor of apoptosis
Alternative Names
API3 antibody, BIRC4 antibody, hIAP 3 antibody, hIAP3 antibody, hILP antibody, IAP 3 antibody, IAP like protein antibody, IAP3 antibody, ILP antibody, ILP1 antibody, MIHA antibody, X linked IAP antibody, XIAP antibody, XLP2 antibody
UniProt ID
P98170
Observed MW
54 kDa
Application
Tested Applications
ELISA, WB, IHC, IF
Recommended dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:100; IF: 1:50 - 1:100
Validated Images
HepG2 cells were subjected to SDS PAGE followed by western blot with FNab09540(XIAP antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded human pancreas cancer using FNab09540(XIAP antibody) at dilution of 1:200
Immunofluorescent analysis of (4% PFA) fixed HeLa cells using FNab09540 (XIAP antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG(H+L)
Background
This gene encodes a protein that belongs to a family of apoptotic suppressor proteins. Members of this family share a conserved motif termed, baculovirus IAP repeat, which is necessary for their anti- apoptotic function. This protein functions through binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2 and inhibits apoptosis induced by menadione, a potent inducer of free radicals, and interleukin 1-beta converting enzyme. This protein also inhibits at least two members of the caspase family of cell-death proteases, caspase-3 and caspase-7. Mutations in this gene are the cause of X-linked lymphoproliferative syndrome. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 2 and 11.