KD-Validated Hsp60 Recombinant Rabbit Monoclonal Antibody

KD-Validated Hsp60 Recombinant Rabbit Monoclonal Antibody

Cat. No.: KVAb01517
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB,FCM,ICC,IHC-P

Reactivity:Human,Mouse,Rat
Conjugate:Unconjugated
Gene Name:HSPD1
Category: KO&KD Validated Antibodies Tags: , , , , , , , , , , ,

Summary

Production Name

KD-Validated Hsp60 Recombinant Rabbit Monoclonal Antibody

Description

KD-Validated antibody

Host

Rabbit

Application

WB,FCM,ICC,IHC-P

Reactivity

Human,Mouse,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Rabbit IgG

Clonality

Rabbit mAb

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

HSPD1

Alternative Names

HSPD1; Heat Shock Protein Family D (Hsp60) Member 1; HSP60; 60 KDa Heat Shock Protein, Mitochondrial; Heat Shock 60kDa Protein 1 (Chaperonin); Mitochondrial Matrix Protein P1; P60 Lymphocyte Protein; 60 KDa Chaperonin; Chaperonin 60; HuCHA60; HSP-60; CPN60; GROEL; SPG13; Spastic Paraplegia 13 (Autosomal Dominant); Epididymis Secretory Sperm Binding Protein; Heat Shock 60kD Protein 1 (Chaperonin); Short Heat Shock Protein 60 Hsp60s1; Heat Shock Protein 65; Heat Shock Protein 60; EC 5.6.1.7; GroEL; HSP65; Hsp60; HLD4

Gene ID

3329

SwissProt ID

P10809

 

Application

Dilution Ratio

WB 1:1,000-1:5,000; FC 1:200-1:2,000; ICC 1:100-1:1,000; IHC-P 1:100-1:200

Molecular Weight

Calculated MW: 61.1kDa

 

Background

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]

 

Research Area

Tags & Cell Markers,Signal Transduction,Kits/ Lysates/ Other

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