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Anti-C22orf9 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Anti-C22orf9 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Catalog # 76121-136
Supplier:  Bioss
Anti-C22orf9 Rabbit Polyclonal Antibody (Alexa Fluor® 750)
Catalog # 76121-136
Supplier:  Bioss
Supplier Number:  BS-9987R-A750
Restricted Products: To process your orders without delay, please provide the required business documentation to purchase this product.

To order chemicals, medical devices, or other restricted products, please provide identification that includes your business name and shipping address via email [email protected] or fax 484.881.5997 referencing your VWR account number. Acceptable forms of identification are:

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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    C22orf9
  • Clonality:
    Polyclonal
  • Conjugation:
    Alexa Fluor® 750
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Western blot:
    Yes
  • Size:
    100 µl
  • Environmentally Preferable:
  • Epitope:
    101-200/404
  • Form:
    Liquid
  • Gene ID:
    23313
  • Antigen synonyms:
    K0930_HUMAN|Chromosome 22 open reading frame 9|KIAA0930|Hypothetical protein LOC23313|Uncharacterized protein C22orf9
  • Modification:
    Unmodified
  • Storage buffer:
    Aqueous buffered solution containing 0.01 M TBS (pH 7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol
  • Storage temperature:
    Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Concentration:
    1 µg/µl
  • Shipping temperature:
    4 °C
  • Immunogen:
    KLH conjugated synthetic peptide derived from human C22orf9
  • Purification:
    Purified by Protein A
  • Cat. no.:
    76121-136
  • Packaging:
    Vial

Specifications

About this item

C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chromosome 22 contains a wide variety of genes with numerous functions. 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.

Type: Primary
Antigen: C22orf9
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 750
Public Immunogen Range: 101-200/404
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat