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SH3BP2 anticorps (AA 400-450)

L’anticorps Lapin Polyclonal anti-SH3BP2 a été validé pour IP. Il convient pour détecter SH3BP2 dans des échantillons de Humain.
N° du produit ABIN7451507

Aperçu rapide pour SH3BP2 anticorps (AA 400-450) (ABIN7451507)

Antigène

Voir toutes SH3BP2 Anticorps
SH3BP2 (SH3-Domain Binding Protein 2 (SH3BP2))

Reactivité

  • 30
  • 12
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Humain

Hôte

  • 25
  • 5
  • 1
Lapin

Clonalité

  • 28
  • 3
Polyclonal

Conjugué

  • 23
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp SH3BP2 est non-conjugé

Application

  • 24
  • 16
  • 7
  • 7
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Immunoprecipitation (IP)
  • Épitope

    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 400-450

    Fonction

    Rabbit anti-SH3BP2 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogène

    between AA 400 and 450

    Isotype

    IgG
  • Indications d'application

    IP: 2 - 10 μg/mg lysate

    WB: Not recommended

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

    Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C

    Date de péremption

    12 months
  • Antigène

    SH3BP2 (SH3-Domain Binding Protein 2 (SH3BP2))

    Autre désignation

    SH3BP2

    Sujet

    Background: SH3 domain-binding protein 2 (SH3BP2) N-terminal pleckstrin homology (PH) domain, an SH3-binding proline-rich region, and a C-terminal SH2 domain. The protein binds to the SH3 domains of several proteins including the ABL1 and SYK protein tyrosine kinases, and functions as a cytoplasmic adaptor protein to positively regulate transcriptional activity in T, natural killer (NK), and basophilic cells. Mutations in this gene result in cherubism, an autosomal dominant inherited syndrome characterized by excessive bone degradation of the upper and lower jaws followed by development of fibrous tissue masses and characteristic facial swelling [taken from NCBI Entrez Gene (Gene ID: 6452)].

    ID gène

    6452

    NCBI Accession

    NP_001116153

    UniProt

    P78314

    Pathways

    TCR Signaling
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