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SLC6A2 (基因名), Sodium-dependent noradrenaline transporter (蛋白名), sc6a2_human.
产品名称:

Human SLC6A2/ Sodium-dependent noradrenaline transporter Recombinant Protein
钠依赖去甲肾上腺素转运体

货号:

R4175h

商标:
EIAab®
监管等级:
别名:

Norepinephrine transporter, Solute carrier family 6 member 2, NET, NAT1, NET1, SLC6A5

序列号:
P23975
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human SLC6A2 Protein
规格 & 价格: cart
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Human SLC6A2 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 16q12.2 by HGNC 16q12.2 by Entrez Gene 16q12.2 by Ensembl
SLC6A2 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Interacts with PRKCABP.


功能:
Amine transporter. Terminates the action of noradrenaline by its high affinity sodium-dependent reuptake into presynaptic terminals.


亚细胞位置:
Cell membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Norepinephrine transporter gene variation modulates acute response to D-amphetamine."

[2].
"Norepinephrine transporter gene (NET) polymorphism in patients with type 2 diabetes."

[3].
"Sequence variations of ABCB1, SLC6A2, SLC6A3, SLC6A4, CREB1, CRHR1 and NTRK2: association with major depression and antidepressant response in Mexican-Americans."

[4].
"Further evidence of association between amphetamine response and SLC6A2 gene variants."

[5].
"Novel and functional norepinephrine transporter protein variants identified in attention-deficit hyperactivity disorder."

[6].
"A haplotype of the norepinephrine transporter (Net) gene Slc6a2 is associated with clinical response to atomoxetine in attention-deficit hyperactivity disorder (ADHD)."

[7].
"Genetic predictors of response to antidepressants in the GENDEP project."

[8].
"Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes."

[9].
"Functional gene variation in the human norepinephrine transporter: association with attention deficit hyperactivity disorder."

[10].
"Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults."
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