C9orf169 antibody

Principal name

C9orf169 antibody

Alternative names for C9orf169 antibody

UPF0574 protein C9orf169, MGC59937

SwissProt ID

A0JNN6 (Bovin), A8MQ03 (Human), Q9D1E4 (Mouse)

Gene ID

375791 (C9orf169)

Available reactivities

Hu (Human)

Available hosts

Rabbit

Available applications

Western blot / Immunoblot (WB), Paraffin Sections (P)

Background of C9orf169 antibody

C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 maps to human chromosome 9q34.3. 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.

2 Item(s)

per page

Proteins & Growth Factors

Catalog No. Species Pres. Purity Source  

C9orf169

C9orf169 Human Purified 12.5% SDS-PAGE Stained with Coomassie Blue.
10 µg / €380.00
  Abnova Taiwan Corp.

C9orf169

C9orf169 Human Purified 12.5% SDS-PAGE Stained with Coomassie Blue.
25 µg / €510.00
  Abnova Taiwan Corp.

2 Item(s)

per page
  • LinkedIn