GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller Mutations in DOK7 are a

Mutations in DOK7 are a cause of familial limb-girdle myasthenia autosomal recessive

Involved in DNA nonhomologous end joining (NHEJ) required for double-strand break (DSB) repair and V(D)J recombination

Three transcript variants encoding different isoforms have been found for CYB5A

this protein is likely involved in hair formation and spermatogenesis in human as well

The opaque black surface reduces background interference from auto ƍuorescence

GTD2B Rabbit Polyclonal Antibody, 100ul Pipette Controller Mutations in DOK7 are aThis gene encodes a glycosylated phosphoprotein with a leucine zipper motif two helix loop helix motifs (I repeats) that are similar to domains found in the TFII I family of transcription factors one CHARLIE8 transposable element like sequence and a BED zinc finger. This gene lies within a region that is deleted in Williams Beuren syndrome. Alternatively spliced variants which encode different protein isoforms have been described; however not all