XPA Polyclonal Antibody, 50ul Organelle Studies Mutations causing Bloom syndrome delete

Mutations causing Bloom syndrome delete or alter helicase motifs and may disable the 3'-5' helicase activity

This kinase has been reported to play roles in many different cellular processes

Perfect for those who like to take risks and push their limits

|tissue specificity:Heart| brain| placenta| lung| liver| skeletal muscle| kidney and pancreas

which hydrolyzes triglycerides and thus provides free fatty acids for cells

XPA Polyclonal Antibody, 50ul Organelle Studies Mutations causing Bloom syndrome deleteXPA encodes a zinc finger protein involved in DNA excision repair. The DNA repair protein complementing XP A cells is part of the NER (nucleotide excision repair) complext which is responsible for repair of UV radiation induced photoproducts and DNA adducts induced by chemical carcinogens. Mutations in this gene are associated with xeroderma pigmentosum complementation group A. Alternatively spliced transcript variants have been found for this gene.