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TRIM37 antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects TRIM37 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN657211

Quick Overview for TRIM37 antibody (C-Term) (ABIN657211)

Target

See all TRIM37 Antibodies
TRIM37 (Tripartite Motif Containing 37 (TRIM37))

Reactivity

  • 27
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 25
  • 1
  • 1
Rabbit

Clonality

  • 26
  • 1
Polyclonal

Conjugate

  • 18
  • 3
  • 2
  • 2
  • 1
  • 1
This TRIM37 antibody is un-conjugated

Application

  • 18
  • 15
  • 5
  • 4
  • 3
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB33250
  • Binding Specificity

    • 7
    • 6
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 936-964, C-Term

    Purification

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

    Immunogen

    This TRIM37 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 936-964 amino acids from the C-terminal region of human TRIM37.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    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

    TRIM37 (Tripartite Motif Containing 37 (TRIM37))

    Alternative Name

    TRIM37

    Background

    This gene encodes a member of the tripartite motif (TRIM) family, whose members are involved in diverse cellular functions such as developmental patterning and oncogenesis. The TRIM motif includes zinc-binding domains, a RING finger region, a B-box motif and a coiled-coil domain. The RING finger and B-box domains chelate zinc and might be involved in protein-protein and/or protein-nucleic acid interactions. The gene mutations are associated with mulibrey (muscle-liver-brain-eye) nanism, an autosomal recessive disorder that involves several tissues of mesodermal origin. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq].

    Molecular Weight

    107906

    NCBI Accession

    NP_001005207, NP_056109

    UniProt

    O94972
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