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Recombinant Rabbit Anti-HSPD1 Monoclonal Antibody
Recombinant Rabbit Anti-HSPD1 Monoclonal Antibody
CPN60; GROEL; HLD4; HSP-60; HSP60; HSP65; HuCHA60; SPG13; 60kDa; HSP-65; Hspd1-30p; CH60_MESAU; HSPD1; 60 kDa chaperonin; Chaperonin 60 (CPN60); Heat shock protein 60 (HSP-60 | Hsp60); Mitochondrial matrix protein P1; 5.6.1.7; CH60_HUMAN; Heat shock prote
Total $295.0
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Regular members: $236.0
  • NO.:SLA0434M
    concentration:1mg/ml
    React Species:Human, Mouse, Rat
    Immunogen Species:Mouse
    Clonality:Monoclonal
    Applications:WB, IHC-P, IHC-F, IF, ELISA
    Gene name:HSPD1
    UniProt Entry:P10809
    NCBI Gene Entry:3329
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Product NameRecombinant Rabbit Anti-HSPD1 Monoclonal Antibody
Cat No.SLA0434M
Chinese Name热休克蛋白-60单克隆抗体
AliasCPN60; GROEL; HLD4; HSP-60; HSP60; HSP65; HuCHA60; SPG13; 60kDa; HSP-65; Hspd1-30p; CH60_MESAU; HSPD1; 60 kDa chaperonin; Chaperonin 60 (CPN60); Heat shock protein 60 (HSP-60 | Hsp60); Mitochondrial matrix protein P1; 5.6.1.7; CH60_HUMAN; Heat shock protein family D member 1; P60 lymphocyte protein; CH60_MOUSE; CH60_RAT; heat shock protein family D (Hsp60) member 1; heat shock 60kD protein 1 (chaperonin); spastic paraplegia 13 (autosomal dominant); heat shock 60kDa protein 1 (chaperonin)
Host SpeciesMouse
IsotypeIgG1
ClonalityMonoclonal
Clone No.2D3
React SpeciesHuman,Mouse,Rat
ApplicationsWB (1:500-2000)
IHC-P (1:100-500)
IHC-F (1:100-500)
IF (1:100-500)
ELISA (1:5000-10000)
Not yet tested in other applications.
Optimal working dilutions must be determined by the end user.
ImmunogenRecombinant human HSP60 Protein
Purificationaffinity purified by Protein A
Concentration1mg/ml
Predicted MW.58 kDa
Subcellular LocationCytoplasm
Gene ID3329
Swiss-ProtP10809
Storage0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
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. Two pseudogenes, both located on chromosome 8, 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.
AttentionThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

 

FOR RESEARCH USE ONLY. Not for use in diagnostic or therapeutic procedures.

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