Brp16 Polyclonal Antibody, 50ul Metabolic enzymes Defects in this gene are

Defects in this gene are a cause of retinitis pigmentosa autosomal recessive (ARRP) disease

Plays a role in receptor-mediated endocytosis via clathrin-coated pits (By similarity)

Transcription factor GATA-4 is thought to regulate genes involved in embryogenesis and in myocardial differentiation and function

The opaque black plate can reduce the background effect caused by auto-ƍuorescence and inter-well interference

but currently do not represent full-length sequences

Brp16 Polyclonal Antibody, 50ul Metabolic enzymes Defects in this gene areBrp16 is a 256 amino acid protein encoded by a gene on human chromosome 8. Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most