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Glyt2 (DGR20922) Rabbit mAb
db11247
Datasheet
- 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. [provided by RefSeq, Jan 2016]
- Immunogen A synthetic peptide of human Glyt2
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Gene ID
9152
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Swiss Prot
Q9Y345
- Synonyms NET1; GLYT2; HKPX3; GLYT-2
- Reactivity Human,Mouse,Rat
- Application WB
- Recommended dilution WB: 1:1000-1:5000
- Calculated MW 87 kDa
- Observed MW 87 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR20922
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Storage/Stability Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
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Western blot detection of Glyt2 in Jurkat,C6 cell lysates using Glyt2 antibody(1:1000 diluted).
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
相关产品
For research use only. Not intended for diagnostic.
