GPD1L Antikörper (AA 1-351)
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- Target Alle GPD1L Antikörper anzeigen
- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
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Bindungsspezifität
- AA 1-351
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Reaktivität
- Human
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Wirt
- Maus
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Klonalität
- Monoklonal
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Konjugat
- Dieser GPD1L Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunofluorescence (IF)
- Immunogen
- Recombinant human GPD1L (1-351aa) purified from E. coli
- Klon
- AT14E2
- Isotyp
- IgG1 kappa
- Top Product
- Discover our top product GPD1L Primärantikörper
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- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Lagerung
- 4 °C,-20 °C,-80 °C
- Informationen zur Lagerung
- Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
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- Target
- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
- Andere Bezeichnung
- GPD1L (GPD1L Produkte)
- Hintergrund
- GPD1L is converts sn-glycerol 3-phosphate to glycerone phosphate. This protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). GPD1L is thought to affect trafficking of the cardiac sodium current to the cell surface. Mutations in GPD1L are the cause of sudden infant death syndrome (SIDS) and Brugada syndrome type 2, an autosomal dominant tachyarrhythmia.
- NCBI Accession
- NP_055956
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