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Glyt2 (PT1132R) PT® Rabbit mAb

商品貨號： PRM8782

適應(yīng) 性： Human,Mouse,Rat

￥800元

規(guī)格：

50ul

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商品描述

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： Glyt2
反應(yīng)性-Reactivity： Human,Mouse,Rat
應(yīng)用-Applications： WB
MW(Calculated)： 88kDa
MW(Observed)： 88kDa
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:1000-1:5000;
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆號： PT1132R
特異性： Endogenous
基因名稱： SLC6A5,GLYT2,NET1
蛋白名稱： Sodium- and chloride-dependent glycine transporter 2 (GlyT-2) (GlyT2) (Solute carrier family 6 member 5)
別名： GLYT2 NET1
Organism-1： Human
基因ID-1： 9152
SwissProt-1： Q9Y345
Organism-2： Mouse
基因ID-2： 104245
SwissProt-2： Q761V0
Organism-3： Rat
基因ID-3： 171148
SwissProt-3： P58295
背景： 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]
細(xì)胞定位： SUBCELLULAR LOCATION: Cell membrane {ECO:0000269|PubMed:16751771, ECO:0000269|PubMed:31370103}; Multi-pass membrane protein {ECO:0000255}.

Glyt2 (PT1132R) PT® Rabbit mAb

Catalog No PRM8782

Product information

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： Glyt2
反應(yīng)性-Reactivity： Human,Mouse,Rat
應(yīng)用-Applications： WB
MW(Calculated)： 88kDa
MW(Observed)： 88kDa
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:1000-1:5000;
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆號： PT1132R
特異性： Endogenous
基因名稱： SLC6A5,GLYT2,NET1
蛋白名稱： Sodium- and chloride-dependent glycine transporter 2 (GlyT-2) (GlyT2) (Solute carrier family 6 member 5)
別名： GLYT2 NET1
Organism-1： Human
基因ID-1： 9152
SwissProt-1： Q9Y345
Organism-2： Mouse
基因ID-2： 104245
SwissProt-2： Q761V0
Organism-3： Rat
基因ID-3： 171148
SwissProt-3： P58295
背景： 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]
細(xì)胞定位： SUBCELLULAR LOCATION: Cell membrane {ECO:0000269|PubMed:16751771, ECO:0000269|PubMed:31370103}; Multi-pass membrane protein {ECO:0000255}.

Hunan UPT Biotechnology Co.,Ltd

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