Order Entry
Belgium
ContactUsLinkComponent
Anti-C9ORF25 Rabbit Polyclonal Antibody (FITC)
Anti-C9ORF25 Rabbit Polyclonal Antibody (FITC)
Catalog # BOSSBS-15324R-FITC
Supplier:  Bioss
Anti-C9ORF25 Rabbit Polyclonal Antibody (FITC)
Catalog # BOSSBS-15324R-FITC
Supplier:  Bioss

Specifications

  • Antibody type:
    Primary
  • Antigen name:
    C9orf25
  • Clonality:
    Polyclonal
  • Conjugation:
    FITC (Fluorescein Isothiocyanate)
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Western blot:
    Yes
  • Epitope:
    1-100/185
  • Form:
    Liquid
  • Gene ID:
    203259
  • Antigen synonyms:
    bA573M23,5|Uncharacterized protein C9orf25|FLJ39031|C9orf25|Hypothetical protein LOC203259|Chromosome 9 open reading frame 25|F219A_HUMAN
  • Modification:
    Unmodified
  • Storage buffer:
    Aqueous buffered solution containing 0,01 M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol
  • Molecular weight:
    20 kDa
  • 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 C9ORF25
  • Tested applications:
    ICC
  • Purification:
    Purified by Protein A
  • Pack type:
    Vial
  • Pk:
    100 µl

Specifications

About this item

C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

Type: Primary
Antigen: C9orf25
Clonality: Polyclonal
Clone:
Conjugation: FITC
Public Immunogen Range: 1-100/185
Host: Rabbit
Isotype: IgG
Reactivity: