HSP60 rabbit pAb

HSP60 rabbit pAb

AO-06-ES2584-100

HSP60 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES2584
Product nameHSP60 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameHSPD1; 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
Size100μL
Unit price ($)248
Human gene ID3329
Human Swiss-ProtP10809
SourceRabbit
IsotypeIgG
TargetHsp60
Fields>>RNA degradation;>>Type I diabetes mellitus;>>Legionellosis;>>Tuberculosis;>>Lipid and atherosclerosis
Gene nameHSPD1
Protein name60 kDa heat shock protein mitochondrial
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID15510
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP63038
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID63868
Rat gene linkView Rat Gene
Rat Swiss-ProtP63039
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human HSP60. AA range:511-560
SpecificityHSP60 Polyclonal Antibody detects endogenous levels of HSP60 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)68kD
BackgroundThis 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],
Functiondisease: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
Subcellular locationMitochondrion matrix.
ExpressionAdipocyte,Adrenal gland,B-cell lymphoma,Brain,Cajal-Retzius

Additional Images

Image 1
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Immunofluorescence analysis of Hela cell. 1,HSP60 Polyclonal Antibody(green) was diluted at 1:200(4° overnight). 2, Goat Anti Rabbit Alexa Fluor 488 Catalog:RS3211 was diluted at 1:1000(room temperature, 50min). 3 DAPI(blue) 10min.
Image 2
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Western Blot analysis of various cells using HSP60 Polyclonal Antibody diluted at 1:2000
Image 3
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Western Blot analysis of COLO205 cells using HSP60 Polyclonal Antibody diluted at 1:2000
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Immunohistochemical analysis of paraffin-embedded Human lung cancer. Antibody was diluted at 1:100(4° overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.
: AO-06-ES2584-100
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