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HSP60 (ABT186) mouse mAb

-YM6884

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Catalog: YM6884
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

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Main Information
Target

Hsp60

Host Species

Mouse

Reactivity

Human, Mouse, Rat,

Applications

IHC, ELISA

MW

60kD (Calculated)

60kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
IHC 1:200-400; ELISA 1:500-5000
Formulation
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Specificity
The antibody can specifically recognize human HSP60 protein.
Purification
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
MW(Calculated)
60kD
MW(Observed)
60kD
Modification
Unmodified
Clonality
Monoclonal
Clone Number
ABT186
Isotype
IgG2b,Kappa
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human HSP60 AA range: 500-573
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Specificity:
The antibody can specifically recognize human HSP60 protein.
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Gene Name:
MAPK7
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Protein Name:
HSP60
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Other Name:
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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Database Link:
Organism Gene ID SwissProt
Human 3329; P10809;
Background:
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],
Function:
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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Cellular Localization:
Cytoplasmic
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Tissue Expression:
Cytoplasmic
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Research Areas:
>>RNA degradation ;
>>Type I diabetes mellitus ;
>>Legionellosis ;
>>Tuberculosis ;
>>Lipid and atherosclerosis
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Catalog: YM6884
Size
Price
Status
Qty.
200μL
$600.00
In stock

0

100μL
$340.00
In stock

0

40μL
$190.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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