GPD1L anticorps (AA 19-351) (Biotin)
Aperçu rapide pour GPD1L anticorps (AA 19-351) (Biotin) (ABIN7994514)
Antigène
Voir toutes GPD1L AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 19-351
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Fonction
- Anti-GPD1L Antibody Biotin Conjugated
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Specificité
- No cross reactivity with other proteins.
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Purification
- Immunogen affinity purified.
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Immunogène
- E.coli-derived human GPD1L recombinant protein (Position: A19-T351).
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Isotype
- IgG
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Indications d'application
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
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Date de péremption
- 12 months
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- GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))
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Autre désignation
- GPD1L
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Sujet
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Background: GPD1L is a human gene. It is mapped to 3p22.3. The protein encoded by this gene contains a glycerol-3-phosphate dehydrogenase (NAD+) motif and shares 72 % sequence identity with GPD1. 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).
Gene Full Name: glycerol-3-phosphate dehydrogenase 1 like
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ID gène
- 23171
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UniProt
- Q8N335
Antigène
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