C9orf174 Polyklonale Antilichaam, PE-Cy5 Vervoeging

Chromosome 9 consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered 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. The KIAA1529 gene product has been provisionally designated KIAA1529 pending further characterization.

BDAG1; Behcet's Disease Associated Gene 1; C9orf174; DKFZp434I2420; DKFZp686B2031; DKFZp686G1725; FLJ41397; FLJ50036; Hypothetical protein LOC100499483; KIAA1529; Uncharacterized protein C9orf174; CI174_HUMAN.

Human, Mouse, Rat

701-800/1646

C9orf174

PE-Cy5

KLH conjugated synthetic peptide derived from human C9orf174

WB

Purified by Protein A.

488nm/670nm

1µg/µl

WB (1:300-5000)

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.