GPD1L (N-term) Rabbit Polyclonal Antibody
CAT#: AP51905PU-N
GPD1L (N-term) rabbit polyclonal antibody, Aff - Purified
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CNY 6160.00
货期*
2周
规格
Specifications
| Product Data | |
| Applications | FC, IHC, WB |
| Recommend Dilution | ELISA: 1/1000. Western Blot: 1/100 - 1/500. Immunohistochemistry on paraffin sections: 1/10 - 1/50. Flow Cytometry: 1/10 - 1/50. |
| Reactivity | Human, Mouse |
| Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | KLH conjugated synthetic peptide between 47-77 amino acids from the N-terminal region of human GPD1L |
| Specificity | This antibody reacts to GPD1L. |
| Isotype | Ig |
| Formulation | PBS State: Aff - Purified State: Liquid purified Ig fraction Preservative: 0.09% (W/V) sodium azide |
| Concentration | lot specific |
| Purification | Affinity chromatography on Protein A |
| Conjugation | Unconjugated |
| Storage Condition | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. |
| Predicted Protein Size | 38419 Da |
| Gene Name | glycerol-3-phosphate dehydrogenase 1-like |
| Database Link | |
| Background | The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS). |
| Synonyms | KIAA0089, GPD1-L |
| Reference Data | |
| Protein Pathways | Glycerophospholipid metabolism |
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