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HSP60 Monoclonal Antibody

商品貨號： PLA004855

適應性： 人,小鼠,大鼠,猴

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

發(fā)貨日期： 7
基因名稱： HSPD1
蛋白名稱： 60 kDa heat shock protein mitochondrial
Human_gene_id： 3329
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=3329
Human_swiss_prot_no： P10809
Human_swiss_link： http://www.uniprot.org/uniprotkb/P10809/entry
Mouse_gene_id： 15510
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=15510
Mouse_swiss_prot_no： P63038
Mouse_swiss_link： http://www.uniprot.org/uniprot/P63038
Rat_gene_id： 63868
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=63868
Rat_swiss_prot_no： P63039
Rat_swiss_link： http://www.uniprot.org/uniprot/P63039
特異性： HSP60 Monoclonal Antibody detects endogenous levels of HSP60 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： HSPD1;HSP60;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
信號通路： RNA degradation;Type I diabetes mellitus;
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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Mitochondrion matrix.
組織表達： Adipocyte,Adrenal gland,B-cell lymphoma,Brain,Cajal-Retzius
科研貨號： PLA004855

HSP60 Monoclonal Antibody

Catalog No PLA004855

Product information

發(fā)貨日期： 7
基因名稱： HSPD1
蛋白名稱： 60 kDa heat shock protein mitochondrial
Human_gene_id： 3329
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=3329
Human_swiss_prot_no： P10809
Human_swiss_link： http://www.uniprot.org/uniprotkb/P10809/entry
Mouse_gene_id： 15510
Mouse_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=15510
Mouse_swiss_prot_no： P63038
Mouse_swiss_link： http://www.uniprot.org/uniprot/P63038
Rat_gene_id： 63868
Rat_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=63868
Rat_swiss_prot_no： P63039
Rat_swiss_link： http://www.uniprot.org/uniprot/P63039
特異性： HSP60 Monoclonal Antibody detects endogenous levels of HSP60 protein.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Monoclonal, Mouse
稀釋： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
純化工藝： Affinity purification
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： HSPD1;HSP60;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
信號通路： RNA degradation;Type I diabetes mellitus;
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.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細胞定位： Mitochondrion matrix.
組織表達： Adipocyte,Adrenal gland,B-cell lymphoma,Brain,Cajal-Retzius
科研貨號： PLA004855

Hunan UPT Biotechnology Co.,Ltd

Website：m.hyjdss.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.