DERL3 Polyclonal Antibody, 20ul Enzymes & Activity Assays Compatible with various disk accessories

Compatible with various disk accessories

Solute carrier family 2 facilitated glucose transporter member 1 is found primarily in the cell membrane and on the cell surface

and mutations in PTHLH are associated with brachydactyly type E2 (BDE2)

The V1 domain consists of three A

A misspliced transcript variant including an intron has been observed in cells from colorectal and pancreatic tumors

DERL3 Polyclonal Antibody, 20ul Enzymes & Activity Assays Compatible with various disk accessoriesThe protein encoded by this gene belongs to the derlin family, and resides in the endoplasmic reticulum (ER). Proteins that are unfolded or misfolded in the ER must be refolded or degraded to maintain the homeostasis of the ER. This protein appears to be involved in the degradation of misfolded glycoproteins in the ER. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene.