Human Glycerol-3-Phosphate Dehydrogenase 1 (GPD1) Protein

Product Graph
338€ (10 µg)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
Human Glycerol-3-Phosphate Dehydrogenase 1 (GPD1) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx690345
tested applications
SDS-PAGE

Description

Human GPD1 Protein is a recombinant protein from Human produced in Human Cells. Recombinant Human Glycerol-3-Phosphate Dehydrogenase [NAD(+)], Cytoplasmic is produced by our Mammalian expression system and the target gene encoding Met1-Met349 is expressed with a 6His tag at the C-terminus.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Proteins and Peptides
Immunogen Target
GPD1
Host
Human
Origin
Human
Observed MW
Molecular Weight: 38.6 kDa

Sequence Fragment: Met1-Met349

Tag: C-terminal 6 His tag

Validity: The validity for this protein is 6 months.
Expression
Recombinant
Purity
> 95% (SDS-PAGE)
Size 1
10 µg
Size 2
50 µg
Tested Applications
SDS-PAGE
Buffer
20mM TrisHCl, 10% Glycerol, pH 8.0.
Availability
Shipped within 5-15 working days.
Storage
Aliquot and store at < -20 °C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P21695
Background
Protein GPD1
Status
RUO
Note
This product is for research use only.   Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

Related Products

EH5162

Human GPD1 (Glycerol-3-phosphate dehydrogenase [NAD(+)]) ELISA Kit

Ver Producto
FNab03579

GPD1 antibody

This gene encodes a member of the NAD-dependent glycerol-3-phosphate dehydrogenase family. The encoded protein plays a critical role in carbohydrate and lipid metabolism by catalyzing the reversible conversion of dihydroxyacetone phosphate (DHAP) and reduced nicotine adenine dinucleotide (NADH) to glycerol-3-phosphate (G3P) and NAD+. The encoded cytosolic protein and mitochondrial glycerol-3-phosphate dehydrogenase also form a glycerol phosphate shuttle that facilitates the transfer of reducing equivalents from the cytosol to mitochondria. Mutations in this gene are a cause of transient infantile hypertriglyceridemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene.

Ver Producto
P4915

Recombinant Human GPD1

Ver Producto