Arg Monoclonal Antibody, 100ul[BT-MCA0181] sgRNA Library Construction Component of the probable SCF(FBXO4)

Component of the probable SCF(FBXO4) complex containing FBXO4

reducing unnecessary pipetting steps

The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme

Catalytic activity:NADH + ubiquinone = NAD(+) + ubiquinol

All CD300L proteins are type I cell surface glycoproteins that contain a single immunoglobulin (Ig) V-like domain

Arg Monoclonal Antibody, 100ul[BT-MCA0181] sgRNA Library Construction Component of the probable SCF(FBXO4)This gene encodes a member of the Abelson family of nonreceptor tyrosine protein kinases. The protein is highly similar to the c abl oncogene 1 protein, including the tyrosine kinase, SH2 and SH3 domains, and it plays a role in cytoskeletal rearrangements through its C terminal F actin and microtubule binding sequences. This gene is expressed in both normal and tumor cells, and is involved in translocation with the ets variant 6 gene in leukemia.