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ITM1472

ITM1472
  • Catalog: ITM1472
  • Gene/Protein: hspd1
  • Product Description: Immunotag™ Hsp60 mouse mAb
405.0000
Price in reward points: 405

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Immunotag™ Hsp60 mouse mAb
Antibody Specification
Datasheet
Target Protein Hsp60
Clonality Monoclonal
Storage/Stability -20°C/1 year
Application WB
Recommended Dilution WB 1:500-2000
Concentration 1 mg/ml
Reactive Species Human,Mouse,Rat,Monkey
Host Species Mouse
Immunogen Recombinant protein corresponding to full length CPN60.
Specificity This antibody detects endogenous levels of Hsp60.
Purification The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
Form Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Gene Name hspd1
Accession No. P10809 P63038
Alternate Names 60 kDa chaperonin ;60 kDa heat shock protein mitochondrial ;60 kDa heat shock protein, mitochondrial ;60kDa ;cb863 ;CH60_HUMAN ;Chaperonin 60 ;Chaperonin ;Chaperonin, 60-KD ;CPN 60 ;CPN60 ;fa04a05 ;fb22d10 ;fi27b05 ;GROEL ;GroEL Homolog ;GroEL, E. coli, homolog of ;Heat shock 60kD protein 1 (chaperonin) ;Heat shock 60kD protein 1 chaperonin ;heat shock 60kDa protein 1 (chaperonin) ;Heat shock 60kDa protein 1 ;Heat shock protein 1 (chaperonin) ;Heat Shock Protein 60 ;Heat shock protein 65 ;HLD4 ;Hsp 60 ;HSP 65 ;HSP-60 ;HSP60 ;HSP65 ;HSPD 1 ;HSPD1 ;HuCHA60 ;id:ibd2197 ;Mitochondrial matrix protein P1 ;P60 lymphocyte protein ;sb:cb144 ;Short heat shock protein 60 Hsp60s1 ;Spastic paraplegia 13 (autosomal dominant) ;Spastic paraplegia 13 ;SPG 13 ;SPG13 ;wu:fa04a05 ;wu:fb22d10 ;wu:fi04a12 ;wu:fi27b05.
Description heat shock protein family D (Hsp60) member 1(HSPD1) Homo sapiens 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],
Cell Pathway/ Category RNA degradation,Type I diabetes mellitus,
Protein Expression Adipocyte,Adrenal gland,B-cell lymphoma,Brain,Cajal-Retzius
Subcellular Localization extracellular space,cytoplasm,mitochondrion,mitochondrial inner membrane,mitochondrial matrix,early endosome,peroxisomal matrix,rough endoplasmic reticulum,Golgi apparatus,cytosol,plasma membrane,clathrin
Protein 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.,
Usage For Research Use Only! Not for diagnostic or therapeutic procedures.
Material Safety Data Sheet
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