EAAT1 Rabbit pAb (一抗) | Bioss

2026-05-01~2026-06-30,AB2605
EAAT1 Rabbit pAb (一抗) | Bioss
货号:bs-1003R
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概述

产品编号
bs-1003R
英文名称
EAAT1 Rabbit pAb
中文名称
胶质细胞谷氨酸运载蛋白1抗体
英文别名
EAA1_HUMAN; SLC1A3; Sodium-dependent glutamate/aspartate transporter 1 (GLAST-1); Solute carrier family 1 member 3; EAAT1; GLAST; GLAST1; EAA1_MOUSE; Glial high affinity glutamate transporter; High-affinity neuronal glutamate transporter (GluT-1); Gmt1; EAA1_RAT; Glial glutamate transporter; Sodium-dependent glutamate/aspartate transporter 1 (GLAST | GLAST-1); solute carrier family 1 (glial high affinity glutamate transporter), member 3; excitatory amino acid transporter 1; glutamate/aspartate transporter 1
抗体来源
Rabbit
免疫原
KLH conjugated synthetic peptide derived from human EAAT1: 301-400/512
亚型
IgG
性状
Liquid
纯化方法
affinity purified by Protein A
克隆类型
Polyclonal
理论分子量
60 kDa
检测分子量
60 kDa
浓度
1mg/ml
储存液
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
SWISS
Gene ID
保存条件
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍
EAAT-1主要用于神经胶质细胞的损伤及退变方面的研究.
背景资料
This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]
胶质细胞谷氨酸运载蛋白1抗体-bs-1003R胶质细胞谷氨酸运载蛋白1抗体-bs-1003R胶质细胞谷氨酸运载蛋白1抗体-bs-1003R胶质细胞谷氨酸运载蛋白1抗体-bs-1003R

产品应用

应用已检合格种属预测种属推荐稀释比例
WBHumanMouse, Rat1:500-2000
IHC-PMouse, RatHuman1:100-500
IHC-FMouse, RatHuman1:100-500
IFMouse, RatHuman1:100-500
Flow-CytHumanMouse, Rat1μg/Test

交叉反应

交叉反应: Human, Mouse, Rat

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靶标

基因名
SLC1A3
蛋白名
Excitatory amino acid transporter 1
亚细胞定位
Membrane; Multi-pass membrane protein
组织特异性
Highly expressed in cerebellum, but also found in frontal cortex, hippocampus and basal ganglia.
翻译后修饰
Glycosylated.
疾病
Defects in SLC1A3 are the cause of episodic ataxia type 6 (EA6) [MIM:612656]. EA6 is characterized by episodic ataxia, seizures, migraine and alternating hemiplegia.
相似性
Belongs to the sodium:dicarboxylate (SDF) symporter (TC 2.A.23) family. SLC1A3 subfamily.
功能
Transports L-glutamate and also L- and D-aspartate. Essential for terminating the postsynaptic action of glutamate by rapidly removing released glutamate from the synaptic cleft. Acts as a symport by cotransporting sodium.

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