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TEX33 antibody (N-Term)

TEX33 Reactivity: Human WB Host: Rabbit Polyclonal RB35923 unconjugated
Catalog No. ABIN1538801
  • Target See all TEX33 products
    TEX33 (Testis Expressed 33 (TEX33))
    Binding Specificity
    • 15
    • 14
    • 7
    AA 1-30, N-Term
    Reactivity
    • 15
    • 14
    Human
    Host
    • 29
    Rabbit
    Clonality
    • 29
    Polyclonal
    Conjugate
    • 5
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TEX33 antibody is un-conjugated
    Application
    • 15
    • 14
    • 13
    • 13
    • 3
    • 3
    • 1
    • 1
    Western Blotting (WB)
    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.
    Clone
    RB35923
    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 (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
    Gene ID
    339669
    NCBI Accession
    NP_001157329, NP_848647
    UniProt
    O43247
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