GPD1L anticorps (N-Term)
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- Antigène Voir toutes GPD1L Anticorps
- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
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Épitope
- AA 47-77, N-Term
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Reactivité
- Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp GPD1L est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
- Specificité
- This antibody reacts to GPD1L.
- Réactivité croisée (Details)
- Species reactivity (tested):Human and Mouse.
- Purification
- Affinity chromatography on Protein A
- Immunogène
- KLH conjugated synthetic peptide between 47-77 amino acids from the N-terminal region of human GPD1L
- Isotype
- Ig Fraction
- Top Product
- Discover our top product GPD1L Anticorps primaire
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.25 mg/mL
- Buffer
- PBS, 0.09 % (W/V) sodium azide
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Conseil sur la manipulation
- Avoid repeated freezing and thawing.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Antigène
- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
- Autre désignation
- GPD1L (GPD1L Produits)
- Synonymes
- anticorps wu:fi13g03, anticorps wu:fi45b08, anticorps zgc:92580, anticorps GPD1-L, anticorps 2210409H23Rik, anticorps D9Ertd660e, anticorps RGD1560123, anticorps glycerol-3-phosphate dehydrogenase 1 like, anticorps glycerol-3-phosphate dehydrogenase 1-like, anticorps glycerol-3-phosphate dehydrogenase 1 like L homeolog, anticorps gpd1l, anticorps GPD1L, anticorps gpd1l.L, anticorps Gpd1l
- Sujet
- 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: GPD1-L, Glycerol-3-phosphate dehydrogenase 1-like protein, KIAA0089
- Poids moléculaire
- 38419 Da
- ID gène
- 23171
- NCBI Accession
- NP_055956
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