PRODUCT NAME

C9orf174 Polyclonal Antibody, Cy7 Conjugated

CONJUGATION

Cy7

HOST

Rabbit

SOURCE

KLH conjugated synthetic peptide derived from human C9orf174

IMMUNOGEN RANGE

CLONALITY

Polyclonal

ISOTYPE

IgG

CONCENTRATION

1ug/ul

PURIFICATION

Purified by Protein A.

STORAGE BUFFER

Aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide.

STORAGE CONDITION

Store at 4°C for 12 months.

GENE ID

SUBCELLULAR LOCATION

SYNONYMS

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

BACKGROUND

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.

APPLICATION DILUTION

IF(IHC-P)(1:50-200)