IkB alpha antibody

Synonyms:I kappa B alpha antibody, IkappaBalpha antibody, IkB alpha antibody, IKBA antibody, Ikβ-α antibody, MAD 3 antibody, MAD3 antibody, NF kappa B inhibitor alpha antibody, NFKBI antibody, NFKBIA antibody
Catalogue No.:FNab04196Reactivity:Human, Mouse, Rat, Pig
Host:RabbitTested Application:ELISA, IHC, IF, WB, IP, FC
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
IkB alpha antibody
Catalogue No.
FNab04196
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
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha
Alternative Names
I kappa B alpha antibody, IkappaBalpha antibody, IkB alpha antibody, IKBA antibody, Ikβ-α antibody, MAD 3 antibody, MAD3 antibody, NF kappa B inhibitor alpha antibody, NFKBI antibody, NFKBIA antibody
UniProt ID
P25963
Observed MW
39 kDa
Application
Tested Applications
ELISA, IHC, IF, WB, IP, FC
Recommended dilution
WB: 1:500-1:2000; IP: 1:500-1:2000; IHC: 1:50-1:500; IF: 1:50-1:500
Validated Images
HL-60 cells were subjected to SDS PAGE followed by western blot with FNab04196(NFKBIA antibody) at dilution of 1:500
IP Result of anti-IkB alpha (IP:FNab04196, 4ug; Detection:FNab04196 1:1000) with HeLa cells lysate 4000ug.
Immunohistochemistry of paraffin-embedded human kidney tissue slide using FNab04196(NFKBIA Antibody) at dilution of 1:200
Immunofluorescent analysis of ( -20℃ Ethanol ) fixed HeLa cells using FNab04196(NFKBIA Antibody) at dilution of 1:50 and Alexa Fluor 488-conjugated Goat Anti-Rabbit IgG(H+L)
Background
This gene encodes a member of the NF-kappa-B inhibitor family, which contain multiple ankrin repeat domains. The encoded protein interacts with REL dimers to inhibit NF-kappa-B/REL complexes which are involved in inflammatory responses. The encoded protein moves between the cytoplasm and the nucleus via a nuclear localization signal and CRM1-mediated nuclear export. Mutations in this gene have been found in ectodermal dysplasia anhidrotic with T-cell immunodeficiency autosomal dominant disease.