HSP60 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA5143537-Each-of-1 | In Stock | ₹ 1,46,494.00 |
PIPA5143537 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 1,46,494.00
GST (18%): ₹ 26,368.92
Total Price: ₹ 1,72,862.92
Antigen
HSP60
Classification
Polyclonal
Conjugate
Unconjugated
Gene
HSPD1
Gene Alias
60 kDa chaperonin; 60 kDa heat shock protein; 60 kDa heat shock protein, mitochondrial; 60kDa; Chaperonin 60; CPN60; GROEL; heat shock 60kD protein 1 (chaperonin); heat shock 60kDa protein 1; heat shock 60kDa protein 1 (chaperonin); Heat shock protein; heat shock protein 1 (chaperonin); heat shock protein 60; heat shock protein 60 (liver); heat shock protein 65; heat shock protein family D (Hsp60) member 1; heat shock protein, 60 kDa; HLD4; HSP; Hsp60; HSP-60; Hsp60s1; HSP65; HSP-65; Hspd1; Hspd1-30p; HuCHA60; hypothetical protein; I79_011398; mitochondrial matrix protein P1; P1 protein; P60 lymphocyte protein; RCJMB04_7g5; short heat shock protein 60 Hsp60s1; SPG13; Unknown (protein for IMAGE:7943409)
Host Species
Chicken
Quantity
500 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgY
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Concentration
Conc. Not Determined
Formulation
PBS with 0.02% sodium azide
Gene Accession No.
P10809, P63038, P63039
Gene Symbols
HSPD1
Immunogen
Recombinant full length human HSP60 expressed in and purified from E. coli
Regulatory Status
RUO
Gene ID (Entrez)
15510, 3329, 63868
Content And Storage
4° C
Form
Liquid
Related Products
Description
- Description 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.