bs-42185P

DATASHEET

Entrez Gene: 91689

Swiss Prot: Q9H4I9

Source: Recombinant human C22orf32 protein is expressed in E.coli with N-Trx-His. It contains the amino acid sequence of 1-64/107

Storage Buffer: 0.01M TBS(pH7.4)

Storage: The product should be stored at -70°C or -20°C.

Background:

Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. The C22orf32 gene product has been provisionally designated C22orf32 pending further characterization

Sequence: 1-64/107

Size: 100ug, 500ug, 20ug

Applications: Others

Mol. Wt.: 24.5

Species: Others

For research use only. Not intended for diagnostic or therapeutic use.