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Merck
CN

MABN504

抗VDAC1 抗体,克隆 N152B/23

clone N152B/23, from mouse

别名:

Voltage-dependent anion-selective channel protein 1, VDAC-1, hVDAC1, Outer mitochondrial membrane protein porin 1, Plasmalemmal porin, Porin 31HL, Porin 31HM

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关于此项目

UNSPSC Code:
12352203
NACRES:
NA.41
eCl@ss:
32160702
Conjugate:
unconjugated
Clone:
N152B/23, monoclonal
Application:
IHC, WB
Citations:
29
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biological source

mouse

conjugate

unconjugated

antibody form

purified antibody

antibody product type

primary antibodies

clone

N152B/23, monoclonal

species reactivity

rat, mouse, human

packaging

antibody small pack of 25 μg

technique(s)

immunohistochemistry: suitable, western blot: suitable

isotype

IgG2aκ

NCBI accession no.

UniProt accession no.

shipped in

ambient

storage temp.

2-8°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... VDAC1(7416)

General description

可观察到约35 kDa的条带
电压依赖性阴离子选择性通道蛋白1(VDAC1,VDAC),也称为线粒体外膜蛋白孔蛋白1,是己糖激酶和BCL2L1的线粒体外膜受体。VDAC1可形成通过线粒体膜的通道,并参与小分子扩散、细胞体积调节和细胞凋亡。VDAC1可能参与渗透性转换孔复合物(PTPC)的形成,该复合物负责线粒体产物的释放,从而触发细胞凋亡。

Immunogen

对应于人VDAC1的重组蛋白。

Application

使用此小鼠单克隆抗体,抗VDAC1抗体,克隆N152B/23,检测VDAC,其已经过验证可用于蛋白质印迹和&IHC。
研究子类别
发育信号转导
研究类别
神经科学
蛋白印迹分析: 代表性批次产品表明VDAC1不与VDAC2或VDAC3发生交叉反应(基于KO验证结果)。代表性批次产品在野生型小鼠肝组织中检测到VDAC1,并使用免疫印迹分析证实了VDAC1敲除小鼠海马组织中的信号丢失(J. Trimmer教授,加州大学戴维斯分校)。
免疫组织化学分析:一个代表性批次产品以1:250的稀释度在人心肌细胞组织中检测到VDAC1。

Biochem/physiol Actions

该抗体不会与VDAC2或VDAC3发生交叉反应(J. Trimmer教授,加州大学戴维斯分校)。

Physical form

形式:纯化
纯化的小鼠单克隆IgG2aκ,溶于含有0.1 M Tris-甘氨酸(pH 7.4,150 mM NaCl)和0.05%叠氮化钠的缓冲液中。
蛋白G纯化

Preparation Note

自发运之日起,在 2-8°C 条件下可稳定保存1年

Analysis Note

对照
小鼠脑组织裂解液
通过蛋白质印迹在小鼠脑组织裂解液中进行了评估。

蛋白质印迹分析:0.5 µg/mL的该抗体可在10 µg小鼠脑组织裂解物中检测到VDAC1。

Other Notes

浓度:请参考批次特异性浓缩物的分析证书。

Disclaimer

除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,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任何类型的消费或应用于人类或动物。

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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)

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Erythropoiesis involves complex interrelated molecular signals influencing cell survival, differentiation, and enucleation. Diseases associated with ineffective erythropoiesis, such as β-thalassemias, exhibit erythroid expansion and defective enucleation. Clear mechanistic determinants of what make erythropoiesis effective are lacking. We previously demonstrated that
Sujung Jun Kim et al.
Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 17(1-2), 228-241 (2021-05-25)
Alzheimer's disease (AD) and other neurodegenerative diseases are characterized by chronic neuroinflammation and a reduction in brain energy metabolism. An important role has emerged for small, non-coding RNA molecules known as microRNAs (miRNAs) in the pathophysiology of many neurodegenerative disorders.
Mitofilin Heterozygote Mice Display an Increase in Myocardial Injury and Inflammation after Ischemia/Reperfusion.
Feng, et al.
Antioxidants (Basel, Switzerland), 12 (2023)
E D'Acunto et al.
Cellular and molecular life sciences : CMLS, 79(8), 437-437 (2022-07-22)
The neurodegenerative condition FENIB (familiar encephalopathy with neuroserpin inclusion bodies) is caused by heterozygous expression of polymerogenic mutant neuroserpin (NS), with polymer deposition within the endoplasmic reticulum (ER) of neurons. We generated transgenic neural progenitor cells (NPCs) from mouse fetal
Hui San Chin et al.
Nature communications, 9(1), 4976-4976 (2018-11-28)
Intrinsic apoptosis is critical to prevent tumor formation and is engaged by many anti-cancer agents to eliminate tumor cells. BAX and BAK, the two essential mediators of apoptosis, are thought to be regulated through similar mechanisms and act redundantly to

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