- ￥2260
- LSM Bio
- 进口
- PAab09992
- 2025年07月15日
- ELISA, WB, IHC
- E. coli - derived recombinant protein
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
PINK1
- 亚型：
IgG
- 形态：
liquid
- 保存条件：
负20摄氏度
- 克隆性：
polyclonal
- 标记物：
Non-conjugated
- 适应物种：
Human
- 保质期：
6个月
- 抗原来源：
Rabbit
- 目录编号：
Q9BZJ3
- 级别：
纯化级别
- 库存：
50
- 供应商：
LSM bio
- 宿主：
E. coli - derived recombinant protein
- 应用范围：
ELISA, WB, IHC
- 浓度：
≥95% as determined by SDS-PAGE
- 靶点：
PINK1
- 抗体英文名：
PINK1 antibody
- 抗体名：
PINK1 antibody
- 规格：
100μl
PINK1 antibody
Product Name PINK1 antibody
Catalog No PAab09992
Packing 100ul
Form liquid
Alternative Name BRPK, PARK6, PINK1, PTEN induced putative kinase 1
Purification Immunogen affinity purified
Purity 95% as determined by SDS-PAGE
Host Rabbit
Isotype IgG
Storage PBS with 0.02% sodium azide and 50% glycerol pH 7.3 , -20Centigrade for 24 months (Avoid repeated freeze / thaw cycles.)
Background/ FUNCTION
This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease.
Immunogen PINK1
Specificity Human
Tested Application ELISA, WB, IHC
Recommended dilution WB: 1:500-1:2000; IHC: 1:50-1:500
IHC use Immunohistochemistry of paraffin-embedded human intestinal cancer using PAab09992(PINK1 antibody) at dilution of 1:100
WB use
Rat heart were subjected to SDS PAGE followed by western blot with PAab09992(PINK1 antibody) at dilution of 1:1000
Protein Information
Gene ID 65018
Uniprot ID Q9BXM7
Calculated MW 30 kDa
Research Area Neuroscience
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文献和实验日本研究人员日前宣布，体内两种基因变异，导致线粒体“次品”在细胞内堆积，是造成青年型帕金森氏症发病的原因。 帕金森氏症患者会出现手脚震颤等运动障碍，给患者的日常生活造成很大困难。目前，日本国内有将近15万名患者，其中大半是老年病人，但其中也有10％左右是40岁以前发病的所谓青年型帕金森氏症患者。 此前的研究表明，如果“Parkin”和“PINK1”这两种基因出现变异，人在年轻时期就会患上帕金森氏症。 东京都临床医学综合研究所与顺天堂大学的研究人员共同研究了上述两种基因。他们发现，两种基因
Generation of Antibody Molecules Through Antibody Engineering
been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional
The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera
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