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IKK-γ Antibody

Familial incontinentia pigmenti (IP) is a genodermatosis that segregates as an X-linked dominant disorder and is usually lethal prenatally in males (The International Incontinentia Pigmenti Consortium, 2000 [PubMed 10839543]). In affected females it causes highly variable abnormalities of the skin, hair, nails, teeth, eyes, and central nervous system.

Alternative Name(s)

FIP-3, FIP3, I-kappa-B kinase gamma, IKBKG, IKK-gamma, IKKAP1, IKKG, IkB kinase gamma subunit, IkB kinase-associated protein 1, Inhibitor of nuclear factor kappa-B kinase gamma subunit, NEMO, NF-kappaB essential modifier, NF-kappaB essential modulator, mF

Application

WB,IF/ICC

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UNIprot

Q9Y6K9

clonality

Polyclonal

reactivity

Human

Research area

Cell Biology

source

Rabbit

storage

Store at -20 ℃. Stable for 12 months from date of receipt.

IKK-γ Antibody

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