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SLC1A1 抗体
SLC1A1
适用: 人
WB, ELISA
宿主: 兔
Polyclonal
unconjugated
SLC1A1抗体详情
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抗原
See all SLC1A1 抗体
SLC1A1
(Solute Carrier Family 1 (Neuronal/epithelial High Affinity Glutamate Transporter, System Xag), Member 1 (SLC1A1))
适用
All reactivities for SLC1A1 抗体
人
宿主
All hosts for SLC1A1 抗体
兔
克隆类型
All clonalities for SLC1A1 抗体
多克隆
标记
All conjugates for SLC1A1 抗体
This SLC1A1 antibody is un-conjugated
应用范围
All applications for SLC1A1 抗体
Western Blotting (WB), ELISA
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Synthetic peptide of human SLC1A1
亚型
IgG
Top Product
Discover our top product SLC1A1 Primary Antibody
Alternatives
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使用细节
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应用备注
WB 1:500-2000, ELISA 1:2000-5000
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
0.4 mg/mL
缓冲液
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
储存液
Sodium azide
注意事项
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
SLC1A1目标详情
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抗原
SLC1A1
(Solute Carrier Family 1 (Neuronal/epithelial High Affinity Glutamate Transporter, System Xag), Member 1 (SLC1A1))
别名
EAAT3 (SLC1A1 产品 )
别名
GB16911 antibody, EAAT3 antibody, SLC1A2a antibody, zgc:91959 antibody, EAAC1 antibody, SCZD18 antibody, D130048G10Rik antibody, EAAC2 antibody, MEAAC1 antibody, Eaac1 antibody, Eaat3 antibody, REAAC1 antibody, excitatory amino acid transporter 3 antibody, solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 antibody, solute carrier family 1 member 1 antibody, LOC412382 antibody, slc1a1 antibody, SLC1A1 antibody, CpipJ_CPIJ000674 antibody, CpipJ_CPIJ001134 antibody, Slc1a1 antibody
背景
This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect.
分子量
57 kDa
NCBI登录号
NP_004161
UniProt
P43005
途径
Dicarboxylic Acid Transport
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