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TRIP12 antibody (AA 991-1023)

The Rabbit Polyclonal anti-TRIP12 antibody has been validated for WB. It is suitable to detect TRIP12 in samples from Human.
Catalog No. ABIN6242961

Quick Overview for TRIP12 antibody (AA 991-1023) (ABIN6242961)

Target

See all TRIP12 Antibodies
TRIP12 (Thyroid Hormone Receptor Interactor 12 (TRIP12))

Reactivity

  • 7
  • 3
  • 3
  • 1
  • 1
  • 1
Human

Host

  • 7
Rabbit

Clonality

  • 7
Polyclonal

Conjugate

  • 7
This TRIP12 antibody is un-conjugated

Application

  • 6
  • 4
  • 3
  • 3
  • 3
  • 2
  • 1
Western Blotting (WB)

Clone

RB54123
  • Binding Specificity

    • 2
    • 2
    • 2
    • 1
    • 1
    AA 991-1023

    Predicted Reactivity

    B, Zf, M, Rat

    Purification

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

    Immunogen

    This TRIP12 antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 991-1023 amino acids from the Central region of human TRIP12.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:2000

    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

    Expiry Date

    6 months
  • Target

    TRIP12 (Thyroid Hormone Receptor Interactor 12 (TRIP12))

    Alternative Name

    TRIP12

    Background

    E3 ubiquitin-protein ligase involved in ubiquitin fusion degradation (UFD) pathway and regulation of DNA repair. Part of the ubiquitin fusion degradation (UFD) pathway, a process that mediates ubiquitination of protein at their N-terminus, regardeless of the presence of lysine residues in target proteins. In normal cells, mediates ubiquitination and degradation of isoform p19ARF/ARF of CDKN2A, a lysine-less tumor suppressor required for p53/TP53 activation under oncogenic stress. In cancer cells, however, isoform p19ARF/ARF and TRIP12 are located in different cell compartments, preventing isoform p19ARF/ARF ubiquitination and degradation. Does not mediate ubiquitination of isoform p16-INK4a of CDKN2A. Also catalyzes ubiquitination of NAE1 and SMARCE1, leading to their degradation. Ubiquitination and degradation of target proteins is regulated by interaction with proteins such as MYC, TRADD or SMARCC1, which disrupt the interaction between TRIP12 and target proteins. Acts as a key regulator of DNA damage response by acting as a suppressor of RNF168, an E3 ubiquitin-protein ligase that promotes accumulation of 'Lys-63'-linked histone H2A and H2AX at DNA damage sites, thereby acting as a guard against excessive spreading of ubiquitinated chromatin at damaged chromosomes.

    Molecular Weight

    220434

    UniProt

    Q14669

    Pathways

    Nuclear Hormone Receptor Binding
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