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|Application / Reactivity||Human|
|Enzyme Immunoassay (EIA)||3 Antibodies|
|Flow Cytometry (FACS)||22 Antibodies|
|Immunochromatography (IC)||3 Antibodies|
|Immunocytochemistry (ICC)||25 Antibodies|
|Immunofluorescence (IF)||36 Antibodies|
|Immunofluorescence (Paraffin-embedded Sections) (IF (p))||51 Antibodies|
|Immunohistochemistry (IHC)||70 Antibodies|
|Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))||45 Antibodies|
|Immunoprecipitation (IP)||5 Antibodies|
|Intracellular Staining (ICS)||1 Antibodies|
|Proximity Ligation Assay (PLA)||1 Antibodies|
|Simple Western (SimWes)||2 Antibodies|
|Western Blotting (WB)||229 Antibodies|
|Antigen||Inhibitor of kappa Light Polypeptide Gene Enhancer in B-Cells, Kinase gamma (IKBKG) Antibodies|
|Conjugate||This IKBKG antibody is un-conjugated Alternatives|
Enzyme Immunoassay (EIA), Western Blotting (WB)
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Product Details anti-IKBKG AntibodyTarget Details IKBKG Application Details Handling Images
|Specificity||This antibody is specific to IKK gamma.|
|Characteristics||Synonyms: FIP3, FIP-3, IKKAP1, I-kappa-B kinase subunit gamma, IKK-gamma, IKKG, IkB kinase subunitgamma, NF-kappa-B essential modulator, NF-kappa-B essential modifier, Inhibitor ofnuclear factor kappa-B kinase subunit gamma, IkB kinase-associated protein 1|
|Purification||Protein G Chromatography eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.|
|Immunogen||This antibody was raised using purified His-tagged recombinant full length human IKKgamma.|
Target Details IKBKGProduct Details anti-IKBKG Antibody Application Details Handling Images back to top
|Alternative Name||NEMO / IKBKG (IKBKG Antibody Abstract)|
|Background||IKK gamma is a regulatory subunit part of the IKK-signalosome complex activation. It is also considered to be a mediator for TAX activation of NF-kappa-B. This protein could be implicated in NF-kappa-B-mediated protection from cytokine toxicity. Defects in IKBKG are the cause of anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID). EDA-ID is a X-linked recessive disorder characterized by absence of sweat glands, sparse scalp hair, rare conical teeth and immunological abnormalities resulting in severe infectious diseases. Defects in IKBKG are the cause of familial incontinentia pigmenti type II (IP2), an X-linked dominant disease causing death in male fetuses. In heterozygous female, it is characterized by disturbance of skin pigmentation sometimes associated with a variety of malformations of the eye, nails, teeth, skeleton, heart, and central nervous system.Synonyms: FIP-3, FIP3, I-kappa-B kinase subunit gamma, IKK-gamma, IKKAP1, IKKG, IkB kinase subunit gamma, IkB kinase-associated protein 1, Inhibitor of nuclear factor kappa-B kinase subunit gamma, NF-kappa-B essential modifier, NF-kappa-B essential modulator|
|Pathways||NF-kappaB Signaling, RTK Signaling, TCR Signaling, TLR Signaling, Fc-epsilon Receptor Signaling Pathway, Activation of Innate immune Response|
Application DetailsProduct Details anti-IKBKG Antibody Target Details IKBKG Handling Images back to top
ELISA: 1/1,000. Western blotting: 1/100-1/500.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.
|Restrictions||For Research Use only|
HandlingProduct Details anti-IKBKG Antibody Target Details IKBKG Application Details Images back to top
|Buffer||PBS containing 0.09 % (W/V) Sodium Azide as preservative.|
|Precaution of Use||This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.|
|Storage||4 °C/-20 °C|
Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer. Avoid repeated freezing and thawing.
Shelf life: one year from despatch.
|Expiry Date||12 months|
ImagesProduct Details anti-IKBKG Antibody Target Details IKBKG Application Details Handling back to top