SOLH1 Rabbit Polyclonal Antibody, 100ul Drying & Desiccation Mutations in STXBP1 have been

Mutations in STXBP1 have been associated with infantile epileptic encephalopathy-4

VitroGel RGD High Concentration comes with VitroGel Dilution Solution (Sucrose-free formulation for cells sensitive to the sugar level in the medium) to adjust the final hydrogel strength from 10 to 4000 Pa

This gene encodes a member of the Fanconi anemia complementation group B

which are integral membrane glycoproteins that participate in the enterohepatic circulation of bile acids

subunit:Found in a complex with SYCE1 and SYCE2

SOLH1 Rabbit Polyclonal Antibody, 100ul Drying & Desiccation Mutations in STXBP1 have beenThis gene encodes one of testis specific transcription factors which are essential for spermatogenesis oogenesis and folliculogenesis. This gene is located on chromosome 9. Mutations in this gene are associated with nonobstructive azoospermia. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.