Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

SH3BP2 antibody (AA 150-200)

This Rabbit Polyclonal antibody specifically detects SH3BP2 in WB and IP. It exhibits reactivity toward Human.
Catalog No. ABIN7450726

Quick Overview for SH3BP2 antibody (AA 150-200) (ABIN7450726)

Target

See all SH3BP2 Antibodies
SH3BP2 (SH3-Domain Binding Protein 2 (SH3BP2))

Reactivity

  • 30
  • 12
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 25
  • 5
  • 1
Rabbit

Clonality

  • 28
  • 3
Polyclonal

Conjugate

  • 23
  • 2
  • 2
  • 2
  • 1
  • 1
This SH3BP2 antibody is un-conjugated

Application

  • 23
  • 16
  • 7
  • 7
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP)
  • Binding Specificity

    • 7
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 150-200

    Purpose

    Rabbit anti-SH3BP2 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 150 and 200

    Isotype

    IgG
  • Application Notes

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    1000 μg/mL

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    4 °C

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    SH3BP2

    Background

    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)].

    Gene ID

    6452

    NCBI Accession

    NP_001116153

    UniProt

    P78314

    Pathways

    TCR Signaling
You are here:
Chat with us!