GPD1L Polyclonal Antibody
| 规格： | / 20μL / 60μL / 120μL / 200μL |
| 价格： | / ￥420 / ￥1010 / ￥1640 / ￥2365 |
货号：E-AB-52905
宿主: Rabbit
反应性: H,M
应用: IHC
Overview
| Synonyms | 2210409H23Rik,D9Ertd660e,Glycerol 3 phosphate dehydrogenase 1 like,Glycerol 3 phosphate dehydrogenase 1 like protein,Glycerol-3-phosphate dehydrogenase 1-like protein,GPD 1L,GPD1-L,gpd1l,GPD1L,KIAA0089,RGD1560123,GPD1L抗体 |
| Swissprot | Q8N335 |
| Source | Rabbit |
| Reactivity | Human, Mouse |
| Immunogen | Fusion protein of human GPD1L |
| Application | IHC(Detection kit: E-IR-R213) |
| Recommended dilution | IHC,,1:50-1:300 |
| Concentration | 1.02mg/mL |
| Clonality | Polyclonal |
Properties
| Cellular localization | Cytoplasm. Localized to the region of the plasma membrane. |
| Isotype | IgG |
| Purification | Affinity purification |
| Conjugation | Unconjugated |
| Storage instructions | Store at -20℃. Avoid freeze / thaw cycles. |
| Storage buffer | PBS with 0.05% NaN3 and 40% Glycerol,pH7.4 |
| 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). |
