SLC6A5 anticorps
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- Antigène Voir toutes SLC6A5 Anticorps
- SLC6A5 (Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5))
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Reactivité
- Rat, Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SLC6A5 est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human SLC6A5
- Isotype
- IgG
- Top Product
- Discover our top product SLC6A5 Anticorps primaire
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- Indications d'application
- WB 1:500 - 1:2000
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 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
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- SLC6A5 (Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5))
- Autre désignation
- SLC6A5 (SLC6A5 Produits)
- Synonymes
- anticorps SLC6A5, anticorps Glyt2, anticorps prestin, anticorps GLYT-2, anticorps GLYT2, anticorps HKPX3, anticorps NET1, anticorps solute carrier family 6 member 5, anticorps solute carrier family 6 (neurotransmitter transporter, glycine), member 5, anticorps SLC6A5, anticorps Slc6a5
- Sujet
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Synonyms: Glycine transporter,Glycine transporter type 2,GlyT-2,GlyT2,NET1,SC6A5,SC6AC5,Slc6a5,SLC6A5 solute carrier family 6 neurotransmitter transporter, glycine member 5,Slc6a9,Sodium and chloride dependent glycine transporter 2,Sodium- and chloride-dependent glycine transporter 2,Solute carrier family 6 member 5,Solute carrier family 6 neurotransmitter transporter glycine member 5
Background: This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia, a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene.
- Poids moléculaire
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Observed_MW: 60kDa
Calculated_MW: 87kDa
- ID gène
- 9152
- UniProt
- Q9Y345
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