跳转至内容
Merck
CN

ABN418

抗-TRPM4抗体

from rabbit, purified by affinity chromatography

别名:

Transient receptor potential cation channel subfamily M member 4, hTRPM4, Calcium-activated non-selective cation, channel 1, Long transient receptor potential channel 4, LTrpC-4, LTrpC4, Melastatin-4

登录 查看组织和合同定价。

选择尺寸


关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

抗-TRPM4抗体, from rabbit, purified by affinity chromatography

biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

purified by

affinity chromatography

species reactivity

human, rat

species reactivity (predicted by homology)

mouse (based on 100% sequence homology), monkey (based on 100% sequence homology), chimpanzee (based on 100% sequence homology)

technique(s)

immunohistochemistry: suitable
western blot: suitable

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

Gene Information

human ... TRPM4(54795)

Analysis Note

通过蛋白质印迹对人小脑组织裂解物进行了评估。

蛋白质印迹分析:0.5 µg/mL该抗体在10 µg人小脑组织裂解物中检测到TRPM4。

Application

免疫组化分析:代表性批次的1:50稀释液在人小脑和人前列腺组织中检测到TRPM4。
抗TRPM4抗体可检测TRPM4的水平&已发布 & 经验证可用于TRPM4。

General description

TRPM4,也称为钙激活非选择性阳离子通道1、长瞬时受体电位通道4、Melastatin-4或LTrpC4,由基因TRPM4/LTRPC4,是一种针对Na+、K+、Cs+和Li+离子的钙激活非选择性离子通道。TRPM4在心肌细胞、皮质和背根神经元、内分泌细胞、肾上皮细胞甚至毛细胞的膜去极化中起着核心作用。此外,TRPM4通过上调β连环蛋白信号通路参与T细胞活化、IL-2产生、血管收缩、胰岛素分泌甚至各种细胞类型的细胞增殖。TRPM4位于细胞膜,高尔基体和内质网。TRPM4广泛表达。TRPM4的缺陷可能与进行性家族性心传导阻滞疾病有关,虽然是不可预测的综合征但可能致命。
观察值〜150 kDa。Uniprot描述了通过在~130 kDa和~147 kDa处选择性剪接产生的2种亚型

Immunogen

对应于N末端附近的人TRPM4的BCP偶联的线性肽。

Other Notes

浓度:请参考批次特异性浓缩物的分析证书。

未找到合适的产品?  

试试我们的产品选型工具.

存储类别

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Jing Yan et al.
Cell reports. Medicine, 5(2), 101413-101413 (2024-02-08)
Toxic signaling by extrasynaptic NMDA receptors (eNMDARs) is considered an important promoter of amyotrophic lateral sclerosis (ALS) disease progression. To exploit this therapeutically, we take advantage of TwinF interface (TI) inhibition, a pharmacological principle that, contrary to classical NMDAR pharmacology
Jiyoung Lee et al.
Nature communications, 11(1), 4283-4283 (2020-09-05)
Our understanding of the spatiotemporal regulation of cardiogenesis is hindered by the difficulties in modeling this complex organ currently by in vitro models. Here we develop a method to generate heart organoids from mouse embryonic stem cell-derived embryoid bodies. Consecutive
Ge Li et al.
mBio, 11(6) (2020-12-10)
Successful treatment of HIV-infected patients with combinational antiretroviral therapies (cART) can now prolong patients' lives to nearly normal life spans. However, the new challenge faced by many of those HIV-infected patients is chronic neuroinflammation and neurotoxicity that often leads to

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持