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Recombinant Phospho-IκB-α (Ser36) Monoclonal Antibody (AN301280L)

Recombinant Phospho-IκB-α (Ser36) Monoclonal Antibody - 1
  • Recombinant Phospho-IκB-α (Ser36) Monoclonal Antibody - 1
  • Recombinant Phospho-IκB-α (Ser36) Monoclonal Antibody - 2
All Size Price Qty
100μL $ 320.00
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50μL $ 211.00
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For research use only.

Verified Samples Verified Samples in IHC: Human colon
Dilution IHC 1:500-1:1000
Isotype IgG,κ
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC
Clonality Monoclonal;Recombinant
Immunogen A synthetic peptide corresponding to residues around (Ser36) of Human Phospho-IκB-α
Abbre IκB-α
Synonyms EDAID,  MAD,  IKBA,  MAD-3,  NFKBI,  IKB alpha,  NFKBIA,  EDAID2,  I kappa B alpha,  IkappaBalpha,  I-kappa-B-alpha,  IKBalpha,  IkB-alpha,  MAD 3,  NF kappa B inhibitor alpha,  MAD3,  alpha,  Major histocompatibility complex enhancer-binding protein MAD3,  NF-kappa-B inhibitor alpha,  Nuclear factor of kappa light chain gene enhancer in B cells,  Nuclear factor of kappa light polypeptide gene enhancer in B cells inhibitor alpha,  nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor,  pIκBα
Swissprot
Cellular Localization Cytoplasm, Nucleus, Shuttles between the nucleus and the cytoplasm by a nuclear localization signal (NLS) and a CRM1-dependent nuclear export.
Concentration 0.2 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A
Research Areas Signal Transduction,  Epigenetics and Nuclear Signaling,  Cancer,  Immunology
Clone No. 9B2
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
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.
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Unconjugated

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