GPD1L Protein (AA 1-351) (His tag)

N° du produit ABIN667561

Détail du produit

Antigène: GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

Type de proteíne: Recombinant

Attributs du protein: AA 1-351

Origine: Humain

Source: Escherichia coli (E. coli)

Purification/Conjugué: Cette GPD1L protéine est marqué à la His tag.

Application: SDS-PAGE (SDS)

Attributs du produit: GPD1L, 1-351aa, Human, His tag, E.coli

Pureté: > 95 % by SDS - PAGE

Information d'application

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/ml (determined by Bradford assay)

Buffer: Liquid. 20mM Tris-HCl buffer (pH8.0) containing 20% glycerol, 1mM DTT

Stock: 4 °C

Détail du antigène

Antigène: GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

Autre désignation: GPD1L (GPD1L Produits)

Synonymes: wu:fi13g03 Protein, wu:fi45b08 Protein, zgc:92580 Protein, GPD1-L Protein, 2210409H23Rik Protein, D9Ertd660e Protein, RGD1560123 Protein, glycerol-3-phosphate dehydrogenase 1 like Protein, glycerol-3-phosphate dehydrogenase 1-like Protein, glycerol-3-phosphate dehydrogenase 1 like L homeolog Protein, gpd1l Protein, GPD1L Protein, gpd1l.L Protein, Gpd1l Protein

Sujet: GPD1L, also known as glycerol-3-phosphate dehydrogenase 1-like protein, converts sn-glycerol 3-phosphate to glycerone phosphate. This protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Mutations in GPD1L are the cause of sudden infant death syndrome (SIDS) and Brugada syndrome type 2, an autosomal dominant tachyarrhythmia. Recombinant human GPD1L protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography. Synonyms: Glycerol-3-phosphate dehydrogenase 1-like protein, GPD1-L. NCBI no.: NP_055956

Poids moléculaire: 40.6 kDa (371aa), confirmed by MALDI-TOF