Description
Product Characteristics:
CTRP2 is a 285 amino acid secreted protein that contains one C1q domain and one collagen-like domain and is encoded by a gene that maps to human chromosome 5. Chromosome 5 contains 181 million base pairs and comprises nearly 6 % of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
Subcellular location: Secreted
Synonyms: C1q and tumor necrosis factor related protein 2, C1QT2_HUMAN, C1qtnf2, Complement C1q tumor necrosis factor-related protein 2, CTRP2, Zacrp2.
Target Information: Please see product details or send an inquiry to antibodies-online for additional target information