Mouse Monoclonal HSP60 antibody [3G8] (STJ98142)

$379.00

Reactivity: Human, Mouse, Rat, Monkey
Applications: WB, IHC, IF, FC, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Mouse Monoclonal HSP60 antibody [3G8] (STJ98142)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, IHC, IF, FC, ELISA

Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody

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HSPD1 antibody, HSP60 antibody,|60 kDa chaperonin antibody|60 kDa heat shock protein, mitochondrial antibody|CH60_HUMAN antibody|Chaperonin 60 antibody|Chaperonin, 60-KD antibody|CPN60 antibody|fa04a05 antibody|GROEL antibody|heat shock 60kDa protein 1 (chaperonin) antibody|Heat shock protein 1 (chaperonin) antibody|Heat shock protein 60 antibody|Heat shock protein 65 antibody|heat shock protein family D (Hsp60) member 1 antibody|HLD4 antibody|Hsp 60 antibody|HSP 65 antibody|HSP-60 antibody|HSP60 antibody|HSP65 antibody|HSPD1 antibody|HuCHA60 antibody|Mitochondrial matrix protein P1 antibody|P60 lymphocyte protein antibody|short heat shock protein 60 Hsp60s1 antibody|SPG13 antibody|Anti-Hsp60 antibody (ab46798)
SCBT cat No: sc-136291|sc-271215|sc-376240|sc-376261|sc-13115|sc-13966|sc-1722|sc-59567|sc-1052|sc-65568|

 

Name

HSP60 Monoclonal Antibody

Catalogue No.

STJ98142

Reactivity

Human, Mouse, Rat, Monkey

Specificity

HSP60 Monoclonal Antibody detects endogenous levels of HSP60 protein.

Immunogen

Purified recombinant fragment of human HSP60 expressed in E Coli

Host

Mouse

Applications

WB, IHC, IF, FC, ELISA

Recommended dilution

WB 1:500-1:2000; IHC 1:200-1:1000; IF 1:200-1:1000; FC 1:200-1:400; ELISA 1:10000

Clonality

Monoclonal

Conjugation

Unconjugated

Isotype

IgG1

Formulation

HSP60 Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.

Concentration

1 mg/ml

Purification

HSP60 Antibody was purified using affinity purification.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

60 kDa heat shock protein, mitochondrial antibody, 60 kDa chaperonin antibody, Chaperonin 60 antibody, CPN60 antibody, Heat shock protein 60 antibody, HSP-60 antibody, Hsp60 antibody, HuCHA60 antibody, Mitochondrial matrix protein P1 antibody, P60 lymphocyte protein antibody

Database links

Human UniProt/Swiss-Prot:P10809;Mouse UniPort/Swiss-Prot: P63038;Rat UniProt/Swiss-Port: P63039;Human Entrez Gene: 3329;Mouse Entrez Gene: 15510;Rat Entrez Gene: Rn.102058

Protein names

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

Protein 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.

Involvement in disease

Spastic paraplegia 13, autosomal dominant (SPG13) [MIM:605280]: A form of spastic paraplegia, a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Leukodystrophy, hypomyelinating, 4 (HLD4) [MIM:612233]: 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 occurs within the first two decades of life. . Note: The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the chaperonin (HSP60) family.

Protein cellular localization

Mitochondrion matrix

Research area

All research areas>Signaling Intermediates>HSP
(View all antibody categories related to Signaling Intermediates)

Note

AntibodyPlus can customize HSP60 Antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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