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 44-73, 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), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This GPD1L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 44-73 amino acids from the N-terminal region of human GPD1L.
- Clone
- RB28552
- Isotype
- Ig Fraction
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- Indications d'application
- WB: 1:1000. IHC-P: 1:50~100. FC: 1:10~50
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 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.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
- Date de péremption
- 6 months
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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).
- Poids moléculaire
- 38419
- ID gène
- 23171
- NCBI Accession
- NP_055956
- UniProt
- Q8N335
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