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TEX33 antibody (N-Term)

The Rabbit Polyclonal anti-TEX33 antibody has been validated for WB. It is suitable to detect TEX33 in samples from Human.
Catalog No. ABIN1538801

Quick Overview for TEX33 antibody (N-Term) (ABIN1538801)

Target

TEX33 (Testis Expressed 33 (TEX33))

Reactivity

  • 15
  • 9
Human

Host

  • 24
Rabbit

Clonality

  • 24
Polyclonal

Conjugate

  • 5
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This TEX33 antibody is un-conjugated

Application

  • 13
  • 13
  • 10
  • 9
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)

Clone

RB35923
  • Binding Specificity

    • 15
    • 9
    • 2
    AA 1-30, N-Term

    Purification

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

    Immunogen

    This EAN57 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human EAN57.

    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

    Storage Comment

    EAN57 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    TEX33 (Testis Expressed 33 (TEX33))

    Alternative Name

    EAN57

    Background

    EAN57 is a 59 amino acid protein encoded by the C22orf33 protein. Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

    Molecular Weight

    30725

    Gene ID

    339669

    NCBI Accession

    NP_001157329, NP_848647

    UniProt

    O43247
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