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TEX33 antibody (N-Term)

TEX33 Reactivity: Human WB, EIA Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN952015
  • Target See all TEX33 products
    TEX33 (Testis Expressed 33 (TEX33))
    Binding Specificity
    • 15
    • 14
    • 7
    AA 1-30, N-Term
    Reactivity
    • 15
    • 15
    Human
    Host
    • 30
    Rabbit
    Clonality
    • 30
    Polyclonal
    Conjugate
    • 6
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TEX33 antibody is un-conjugated
    Application
    • 15
    • 15
    • 13
    • 13
    • 4
    • 3
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    Specificity
    This antibody recognizes Human EAN57 / C22orf33 (N-term).
    Purification
    Affinity Chromatography on Protein A
    Immunogen
    KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of Human EAN57
    Isotype
    Ig Fraction
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.25 mg/mL
    Buffer
    PBS containing 0.09 % (W/V) Sodium Azide as preservative
    Preservative
    Sodium azide
    Precaution of Use
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handling Advice
    Avoid repeated freezing and thawing.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
  • Target
    TEX33 (Testis Expressed 33 (TEX33))
    Alternative Name
    EAN57 / C22orf33 (TEX33 Products)
    Synonyms
    C22orf33 antibody, EAN57 antibody, cE81G9.2 antibody, 1700061J05Rik antibody, Ean57 antibody, testis expressed 33 antibody, TEX33 antibody, Tex33 antibody
    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 Da
    Gene ID
    339669
    NCBI Accession
    NP_001157329
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