Recombinant Human HSPD1 / HSP60 Protein (His & GST tag) 100µg

Product information

  • Size

    100µg

  • Catalog number

    PKSH031150-100µg

  • Price

    626 EUR

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Recombinant Human HSPD1 / HSP60 Protein (His & GST tag) 100µg
on Gentaurs online shop

Product details

Synonym

CPN60;GROEL;HLD4;HSP-60;HSP60;HSP65;HuCHA60;SPG13

Activity

NA

Sequence

Leu 2-Phe 573

Fusion tag

N-His & GST

Accession

NP_955472.1

Expressed Host

E. coli

Shipping

In general, recombinant proteins are provided as lyophilized powder which are shipped at ambient temperature.Bulk packages of recombinant proteins are provided as frozen liquid. They are shipped out with blue ice unless customers require otherwise.

Purity

＞90 % as determined by SDS-PAGE

Endotoxin

Please contact us for more information.

Stability and Storage

Samples are stable for up to twelve months from date of receipt at -70℃.Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.

Mol Mass

88.7 kDa

AP Mol Mass

52-65 kDa

Formulation

Lyophilized from sterile PBS, pH 7.4

Reconstitution

Please refer to it for detailed information.

Background

HSPD1, also known as HSP60, is a member of the chaperonin family. HSPD1 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. It may also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix. HSPD1 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. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13.Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13). Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Defects in HSPD1 are the cause of leukodystrophy hypomyelinating type 4 (HLD4); also called mitochondrial HSP60 chaperonopathy or MitCHAP-60 disease. HLD4 is a severe autosomal recessive hypomyelinating leukodystrophy. HSPD1 is cinically characterized by infantile-onset rotary nystagmus, progressive spastic paraplegia, neurologic regression, motor impairment, profound mental retardation. Death usually occurrs within the first two decades of life.Immune Checkpoint   Immunotherapy   Cancer Immunotherapy   Targeted Therapy

Conjugation

histidine

Properties

Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.

Source

Recombinants or rec. proteins

Group

recombinants

Click to buy
Recombinant Human HSPD1 / HSP60 Protein (His & GST tag) 100µg
on Gentaurs online shop