GPD2 Rabbit Polyclonal Antibody
Specifications
| Product Data | |
| Application | IHC, WB |
|---|---|
| Recommended Dilution | WB: 500-2000 WB positive control: A172, 231 and Hela cells IHC: 20-100 Positive control: Human esophagus cancer Predicted cell location: Cytoplasm |
| Reactivity | Human, Mouse, Rat |
| Antibody Host | Rabbit |
| Isotype | IgG |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide of human GPD2 |
| Buffer | pH7.4 PBS, 0.05% NaN3, 40% Glyceroln |
| Concentration | lot specific |
| Purification | Antigen affinity purification |
| Conjugation | Unconjugated |
| Storage | Store at -20°C as received. |
| Stability | Stable for 12 months from date of receipt. |
| Shipping | Blue Ice |
| Predicted Protein Size | 81 kDa |
| Gene Name | glycerol-3-phosphate dehydrogenase 2 |
| Database Link | |
| Background | The protein encoded by this gene localizes to the inner mitochondrial membrane and catalyzes the conversion of glycerol-3-phosphate to dihydroxyacetone phosphate, using FAD as a cofactor. Along with GDP1, the encoded protein constitutes the glycerol phosphate shuttle, which reoxidizes NADH formed during glycolysis. Two transcript variants encoding the same protein have been found for this gene. |
| Synonyms | GDH2; GPDM; mGPDH |
| Reference Data | |
| Protein Categories | Intracellular Proteins |
| Protein Families | Druggable Genome, Transmembrane |
| Protein Pathways | Glycerophospholipid metabolism |
Reviews
Documents
| Product Manuals |
| FAQs |
| SDS |
Citations
Administration of chitosan-tripolyphosphate-DNA nanoparticles to knockdown glutamate dehydrogenase expression impairs transdeamination and gluconeogenesis in the liver
Gaspar, Silva-Marrero, Fàbregas et al
J. Biotechnol. (2018) 286, 5-13 DOI: 10.1016/j.jbiotec.2018.09.002
Gaspar, Silva-Marrero, Fàbregas et al
J. Biotechnol. (2018) 286, 5-13 DOI: 10.1016/j.jbiotec.2018.09.002
AI Summary: OriGene contributed to this study by providing the rabbit anti-GDH antibody, which was used to detect glutamate dehydrogenase protein levels in liver samples during the assessment of GDH knockdown efficiency.
Snippet: onto a polyvinylidene fluoride membrane for 3 hours at 60 V and 4 °C. After incubation in blocking buffer (non-fat skim milk powder 5 % w/v, 50 mM Tris-base pH 7.5, 100 mM NaCl, 0.1 % Tween 20), the membrane was exposed to rabbit anti-GDH (OriGene, Rockville
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