SLC6A5 Antikörper
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- Target Alle SLC6A5 Antikörper anzeigen
- SLC6A5 (Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5))
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Reaktivität
- Ratte, Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser SLC6A5 Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB)
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant protein of human SLC6A5
- Isotyp
- IgG
- Top Product
- Discover our top product SLC6A5 Primärantikörper
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- Applikationshinweise
- WB 1:500 - 1:2000
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- SLC6A5 (Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5))
- Andere Bezeichnung
- SLC6A5 (SLC6A5 Produkte)
- Synonyme
- SLC6A5 antikoerper, Glyt2 antikoerper, prestin antikoerper, GLYT-2 antikoerper, GLYT2 antikoerper, HKPX3 antikoerper, NET1 antikoerper, solute carrier family 6 member 5 antikoerper, solute carrier family 6 (neurotransmitter transporter, glycine), member 5 antikoerper, SLC6A5 antikoerper, Slc6a5 antikoerper
- Hintergrund
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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.
- Molekulargewicht
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Observed_MW: 60kDa
Calculated_MW: 87kDa
- Gen-ID
- 9152
- UniProt
- Q9Y345
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