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Reconstitute at 0.2 mg/mL in sterile PBS.
Multiple coagulation factor deficiency protein 2 (MCFD2) is localized in the endoplasmic reticulum-Golgi intermediate compartment (ERGIC) through a direct, calcium-dependent interaction with LMAN1. The MCFD2-LMAN1 complex forms a specific cargo receptor for the transport of selected proteins from the endoplasmic reticulum to the Golgi apparatus. Mutations in the MCFD2 gene may cause of factor V and factor VIII combined deficiency (F5F8D). F5F8D is an autosomal recessive human bleeding disorder characterized by the reduction of both clotting proteins.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Multiple coagulation factor deficiency protein 2 homolog; neural stem cell derived neuronal survival protein; Neural stem cell-derived neuronal survival protein
基因别名: 1810021C21Rik; F5f8d; Lman1ip; Mcfd2; Sdnsf
UniProt ID: (Mouse) Q8K5B2
Entrez Gene ID: (Mouse) 193813