C1orf122 antibody

Principal name

C1orf122 antibody

Alternative names for C1orf122 antibody


SwissProt ID

B1ARW8 (Mouse), Q6ZSJ8 (Human)

Gene ID

127687 (C1orf122)

Available reactivities

Hu (Human)

Available hosts


Available applications

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

Background of C1orf122 antibody

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf122 gene product has been provisionally designated C1orf122 pending further characterization.

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Primary Antibodies

Catalog No. Host Iso. Clone Pres. React. Applications  

C1orf122 antibody

C1orf122 Rabbit IgG Purified Hu WB
  OriGene Technologies, Inc.

C1orf122 (N-term) antibody

C1orf122 Rabbit Aff - Purified Hu WB
  AVIVA Systems Biology

C1orf122 antibody

C1orf122 Rabbit Aff - Purified Hu WB
  Novus Biologicals Inc.

3 Item(s)

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