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TBL2 antibody (N-Term)

This anti-TBL2 antibody is a Rabbit Polyclonal antibody detecting TBL2 in WB and IHC (p). Suitable for Human.
Catalog No. ABIN2845981

Quick Overview for TBL2 antibody (N-Term) (ABIN2845981)

Target

See all TBL2 Antibodies
TBL2 (Transducin (Beta)-Like 2 (TBL2))

Reactivity

  • 23
  • 4
  • 2
  • 2
  • 2
Human

Host

  • 21
  • 2
Rabbit

Clonality

  • 23
Polyclonal

Conjugate

  • 18
  • 1
  • 1
  • 1
  • 1
  • 1
This TBL2 antibody is un-conjugated

Application

  • 22
  • 11
  • 11
  • 3
  • 3
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB32541
  • Binding Specificity

    • 8
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 43-72, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This TBL2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 43-72 amino acids from the N-terminal region of human TBL2.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

    Storage Comment

    TBL2 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Expiry Date

    6 months
  • Target

    TBL2 (Transducin (Beta)-Like 2 (TBL2))

    Alternative Name

    TBL2

    Background

    This gene encodes a member of the beta-transducin protein family. Most proteins of the beta-transducin family are involved in regulatory functions. This protein is possibly involved in some intracellular signaling pathway. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23.

    Molecular Weight

    49798

    Gene ID

    26608

    NCBI Accession

    NP_036585

    UniProt

    Q9Y4P3
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