Overview |
bs-15324R-PE-Cy3 |
C9orf25 Polyclonal Antibody, PE-Cy3 Conjugated |
WB |
Human, Mouse, Rat, Sheep, Horse, Chicken |
Specifications |
PE-Cy3 |
Rabbit |
KLH conjugated synthetic peptide derived from human C9orf25 |
1-100/185 |
Polyclonal |
IgG |
1ug/ul |
Purified by Protein A. |
Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol. |
Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles. |
Target |
203259 |
Nucleus |
bA573M23.5; C9orf25; Chromosome 9 open reading frame 25; F219A_HUMAN; FLJ39031; Hypothetical protein LOC203259; Uncharacterized protein C9orf25. |
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 characterized 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. |
Application Dilution |
WB |
1:300-5000 |