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HSP60 (ABT186) mouse mAb (Ready to Use)

-YM6884R

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货号: YM6884R
规格
价格
货期
数量
10mL
¥1,200.00
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6mL
¥900.00
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3mL
¥600.00
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主要信息
Target

Hsp60

Host Species

Mouse

Reactivity

Human, Mouse, Rat,

Applications

IHC

Conjugate/Modification

Unmodified

详细信息
推荐稀释比
Ready to use for IHC
组成
The prediluted ready-to-use antibody is diluted in phosphate buffer saline containing stabilizing protein and 0.05% Proclin 300
特异性
The antibody can specifically recognize human HSP60 protein.
纯化工艺
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
储存
2°C to 8°C/1 year
修饰
Unmodified
克隆性
Monoclonal
克隆号
ABT186
同种型
IgG2b,Kappa
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抗原&靶点信息
免疫原:
Synthesized peptide derived from human HSP60 AA range: 500-573
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特异性:
The antibody can specifically recognize human HSP60 protein.
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基因名称:
MAPK7
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蛋白名称:
HSP60
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别名:
60 kDa heat shock protein, mitochondrial ;
60 kDa chaperonin ;
Chaperonin 60 ;
CPN60 ;
Heat shock protein 60 ;
HSP-60 ;
Hsp60 ;
HuCHA60 ;
Mitochondrial matrix protein P1 ;
P60 lymphocyte protein ;
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数据库链接:
Organism 基因 ID SwissProt
Human 3329; P10809;
背景:
This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun 2010],
功能:
Disease:Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13) [MIM:605280]. Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs.,Disease:Defects in HSPD1 are the cause of leukodystrophy hypomyelinating type 4 (HLD4) [MIM:612233]; also called mitochondrial HSP60 chaperonopathy or MitCHAP-60 disease. HLD4 is a severe autosomal recessive hypomyelinating leukodystrophy. Clinically characterized by infantile-onset rotary nystagmus, progressive spastic paraplegia, neurologic regression, motor impairment, profound mental retardation. Death usually occurrs within the first 2 decades of life.,Function:Implicated in mitochondrial protein import and macromolecular assembly. May facilitate the correct folding of imported proteins. May also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix.,similarity:Belongs to the chaperonin (HSP60) family.,similarity:Belongs to the TCP-1 chaperonin family.,subunit:Interacts with HBV protein X and HTLV-1 protein p40tax.,
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细胞定位:
Cytoplasmic
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组织表达:
Cytoplasmic
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研究领域:
>>RNA degradation ;
>>Type I diabetes mellitus ;
>>Legionellosis ;
>>Tuberculosis ;
>>Lipid and atherosclerosis
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货号: YM6884R
规格
价格
货期
数量
10mL
¥1,200.00
现货

0

6mL
¥900.00
现货

0

3mL
¥600.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询

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