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Merck
CN

MAB5502

抗-囊泡谷氨酸转运体1抗体

CHEMICON®, mouse monoclonal, 3C10.2

别名:

Solute carrier family 17 member 7, Brain-specific Na(+)-dependent inorganic phosphate cotransporter, vGluT1

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关于此项目

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41
Clone:
3C10.2, monoclonal
Species reactivity:
mouse
Application:
IHC, WB
Citations:
76
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产品名称

抗-囊泡谷氨酸转运体1抗体, clone 3C10.2, Chemicon®, from mouse

biological source

mouse

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

3C10.2, monoclonal

species reactivity

mouse

species reactivity (predicted by homology)

rat

manufacturer/tradename

Chemicon®

technique(s)

immunohistochemistry: suitable, western blot: suitable

isotype

IgG1

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

Gene Information

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General description

60 kDa
VGLUT1在谷氨酸神经元的子集中表达,并将谷氨酸从大脑转运到天然突触小泡中,表现出被谷氨酸阻断的氯化物电导。囊泡谷氨酸转运具有比质膜兴奋性氨基酸转运蛋白低得多的表观亲和力。VGLUT1的谷氨酸转运被约2 mM的K(m)饱和,与突触小泡的转运范围相同。最后,质膜谷氨酸转运蛋白将天冬氨酸和谷氨酸都识别为底物,而VGLUT1不识别天冬氨酸。 囊泡谷氨酸转运蛋白将神经递质包装到突触小泡中,以便它们可以释放到突触中。VGLUT依赖于它们通过水解三磷酸腺苷(ATP)产生的质子梯度。VGLUT对谷氨酸的亲和力仅为EAAT的百分之一至千分之一。

Immunogen

来自大鼠VGLUT1的重组蛋白。

Application

免疫组织化学:
通过IH检验了该抗体的一个先前批次。

最佳工作稀释度必须由最终用户确定。
研究子类别
离子通道&转运蛋白

神经元&神经胶质标志物
研究类别
神经科学
该抗囊泡谷氨酸转运蛋白1抗体,克隆3C10.2,目录号MAB5502,经验证可用于IH、WB检测VGluT1。

Biochem/physiol Actions

与VGLUT1(囊泡谷氨酸转运蛋白1)反应。

Physical form

形式:纯化
纯化的小鼠单克隆IgG1,溶于含0.1%叠氮化钠的PBS的缓冲液中。
纯化蛋白A

Preparation Note

自收到之日起以未稀释的等分试样形式,在2-8ºC可稳定保存6个月。

Analysis Note

对照


VGLUT1对照肽AG208
通过蛋白质印迹法对小鼠脑裂解物进行常规评估。

蛋白质印迹分析:
该批次以1:500稀释度在10 μg小鼠脑裂解物中检测到囊泡谷氨酸转运蛋白1。

Other Notes

浓度:关于批次特定浓度请参见检验报告。

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

除非我们的目录或产品随附的其他公司文件中另有说明,否则我们的产品预期仅用于研究用途,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或对人类或动物的任何类型的消费或应用。

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存储类别

12 - Non Combustible Liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Spiral ganglion neurons (SGNs) are usually damaged in sensorineural hearing loss. SGN-derived neural stem cells (NSCs) have been identified and proposed to differentiate into neurons to replace damaged SGNs. However, it remains obscure whether SGN-NSC-derived neurons (ScNs) are electrophysiologically functional
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