89-110-441

HSPD1, Mouse, Clone: SJ-60, Abnova™

Manufacturer: Abnova Corporation

Select a Size

Pack Size SKU Availability Price
Each of 1 89-110-441-Each-of-1 In Stock ₹ 68,797.00

89-110-441 - Each of 1

₹ 68,797.00

In Stock

Quantity

1

Base Price: ₹ 68,797.00

GST (18%): ₹ 12,383.46

Total Price: ₹ 81,180.46

Antigen

HSPD1

Classification

Monoclonal

Conjugate

Unconjugated

Dilution

Western Blot (2-4 ug/mL) Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (4-8 ug/mL) The optimal working dilution should be determined by the end user.

Gene

HSPD1

Gene Symbols

HSPD1

Immunogen

Recombinant protein corresponding to full length human HSPD1.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human

Form

Lyophilized

Applications

Immunohistochemistry (PFA fixed), Western Blot

Clone

LK1

Description

Mouse monoclonal antibody raised against full length recombinant HSPD1.

Formulation

Lyophilized from 1.2% sodium acetate (2mg BSA, 0.01mg sodium azide)

Gene Alias

CPN60/GROEL/HLD4/HSP60/HSP65/HuCHA60/SPG13

Host Species

Mouse

Purification Method

Affinity purification

Regulatory Status

RUO

Gene ID (Entrez)

3329

Content And Storage

Store at -20°C on dry atmosphere. After reconstitution with 1mL of 1.2% sodium acetate or neutral PBS to a concentration of 100μg/mL store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

Isotype

IgG1

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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
  • 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
  • [provided by RefSeq