GPD1 Recombinant Rabbit Monoclonal Antibody (HL1959), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA550354-Each-of-1 | In Stock | ₹ 41,385.00 |
FEMA550354 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 41,385.00
GST (18%): ₹ 7,449.30
Total Price: ₹ 48,834.30
Antigen
GPD1
Classification
Recombinant Monoclonal
Concentration
1 mg/mL
Formulation
PBS with no preservative
Gene Accession No.
O35077, P13707, P21695
Gene Symbols
Gpd1
Immunogen
Recombinant protein encompassing a sequence within the C-term region of human GPD1. The exact sequence is proprietary.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Clone
HL1959
Conjugate
Unconjugated
Gene
Gpd1
Gene Alias
AI747587, Gdc1, Gdc-1, glycerol 3-phosphate dehydrogenase, glycerol phosphate dehydrogenase 1, cytoplasmic adult, Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, glycerol-3-phosphate dehydrogenase [NAD+], cytoplasmic, glycerol-3-phosphate dehydrogenase 1, glycerol-3-phosphate dehydrogenase 1 (soluble), glycerolphosphate dehydrogenase 1, cytoplasmic adult, glycerophosphate dehydrogenase, Gpd1, Gpd3, GPD-C, GPDH, GPDH-C, HTGTI, Kiaa4010, mKIAA4010
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
14555, 2819, 60666
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Isotype
IgG
Related Products
Description
- 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.