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Recombinant Human ATP2C1 Protein, N-GST

Catalog #:   YHF80501 Specific References (50) DATASHEET
Applications: ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Expression system: E. coli
Accession: P98194
Protein length: Met1-Pro70
Overview

Catalog No.

YHF80501

Expression system

E. coli

Species

Homo sapiens (Human)

Protein length

Met1-Pro70

Predicted molecular weight

34.72 kDa

Nature

Recombinant

Endotoxin level

Please contact with the lab for this information.

Purity

>90% as determined by SDS-PAGE.

Accession

P98194

Applications

ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress

Form

Lyophilized

Storage buffer

Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.

Reconstitution

Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.

Shipping

In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.

Stability and Storage

Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.

Alternative Names

Calcium-transporting ATPase type 2C member 1, ATP-dependent Ca(2+) pump PMR1, PMR1L, KIAA1347, ATP2C1, ATPase 2C1

Data Image
  • SDS-PAGE
    SDS PAGE for recombinant Human ATP2C1
References

Tofacitinib as a promising treatment for refractory erythroderma-like Hailey-Hailey disease., PMID:40298163

Targeting the secretory program of 3q-amplified lung cancers., PMID:40047887

Chemigenetic Ca2+ indicators report elevated Ca2+ levels in endothelial Weibel-Palade bodies., PMID:39869616

Hailey-Hailey disease successfully treated with naloxone: 2 case reports and Review of the literature on efficacy of opioid receptor antagonist in Hailey-Hailey disease patients., PMID:39842790

Hailey-Hailey Disease Caused by a Novel Deep Intronic Variant in ATP2C1., PMID:39523677

Adipocytes reprogram the proteome of breast cancer cells in organotypic three-dimensional cell cultures., PMID:39505903

Biochemical and molecular responses to long-term salinity challenges in northern quahogs Mercenaria mercenaria., PMID:39250983

Increased risk of cardiac arrhythmia in Hailey-Hailey disease patients., PMID:39241028

Deciphering glial contributions to CSF1R-related disorder via single-nuclear transcriptomic profiling: a case study., PMID:39217398

Pumping the Breaks on Acantholytic Skin Disorders: Targeting Calcium Pumps, Desmosomes, and Downstream Signaling in Darier, Hailey-Hailey, and Grover Disease., PMID:39207315

Generalized Hailey-Hailey disease associated with c.2395C>T ATP2C1 gene mutation and fatal outcome., PMID:38959923

ATP2C1 knockdown induces abnormal expressions of cytoskeletal and tight junction proteins mimicking Hailey-Hailey disease., PMID:38841932

Hailey-Hailey disease: clinical, diagnostic and therapeutic update., PMID:38789364

A case of Hailey-Hailey disease with novel ATP2C1 gene variant (c.G925C) showing unusual phenotype., PMID:38711270

Chromosomal 3q amplicon encodes essential regulators of secretory vesicles that drive secretory addiction in cancer., PMID:38662435

A novel ATP2C1 mutation (c.1840-1G>A) in a sporadic case of isolated perianal Hailey-Hailey disease with human papillomavirus type 58 infection., PMID:38637183

Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency., PMID:38335567

Two patients with Hailey-Hailey disease with novel pathogenic ATP2C1 variants suggesting possible genotype/phenotype correlations., PMID:38111361

Hailey-Hailey Disease is Associated with Diabetes: A Population-based Cohort Study, Clinical Cohort Study, and Pedigree Analysis., PMID:38014829

[Establishment of a prostate cancer prognostic risk model based on the TCGA database and inflammation-related genes]., PMID:37846114

Hailey-Hailey disease successfully treated with photodynamic therapy: Case report., PMID:37558191

Tetramethylpyrazine ameliorates endotoxin-induced acute lung injury by relieving Golgi stress via the Nrf2/HO-1 signaling pathway., PMID:37550659

Ultrashort wave alleviates oxygen-glucose deprivation/reoxygenation injury via up-regulation of SPCA1 expression in N2a cells., PMID:37539566

Two Novel and a Recurrent ATP2C1 Mutations in Chinese Population with Hailey-Hailey Disease., PMID:37342538

ZNF384-Related Fusion Genes in Acute Lymphoblastic Leukemia., PMID:37306722

Two sporadic cases of childhood-onset Hailey-Hailey disease with superimposed mosaicism., PMID:36922631

Cryo-EM structures of human SPCA1a reveal the mechanism of Ca2+/Mn2+ transport into the Golgi apparatus., PMID:36867705

Loss of ATP2C1 function promotes trafficking and degradation of NOTCH1: Implications for Hailey-Hailey disease., PMID:36789506

GARP dysfunction results in COPI displacement, depletion of Golgi v-SNAREs and calcium homeostasis proteins., PMID:36578782

Subcellular compartmentalization of STIM1 for the distinction of Darier disease from Hailey-Hailey disease., PMID:36442136

Anti-desmoglein 1 antibody-positive mother and antibody-negative child with Darier's disease., PMID:36074695

Calcium and the Ca-ATPase SPCA1 modulate plasma membrane abundance of ZIP8 and ZIP14 to regulate Mn(II) uptake in brain microvascular endothelial cells., PMID:35787370

Two novel mutations in the ATP2C1 gene found in Japanese patients with Hailey-Hailey disease., PMID:35274376

Two cases of Hailey-Hailey disease effectively treated with apremilast and a review of reported cases., PMID:34569085

Role of pro-inflammatory cytokines in the pathophysiology of herpes simplex virus superinfection in Darier's disease., PMID:34355821

Weak immunohistochemical expression of galectin-3 near blisters in Hailey-Hailey disease., PMID:34272745

Identification of novel potential interaction partners of UDP-galactose (SLC35A2), UDP-N-acetylglucosamine (SLC35A3) and an orphan (SLC35A4) nucleotide sugar transporters., PMID:34242836

Papular acantholytic dyskeratosis of the anogenital area with novel ATP2C1 gene mutations., PMID:34134127

Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain., PMID:33926923

Whole exome sequencing improves mutation detection in Hailey-Hailey disease., PMID:33878236

Crosstalk among Calcium ATPases: PMCA, SERCA and SPCA in Mental Diseases., PMID:33801794

A novel deletion mutation in the ATP2C1 gene in a case of generalized Hailey-Hailey disease possibly aggravated by scabies infection., PMID:33580912

Elderly-onset type 1 mosaic form of Hailey-Hailey disease with a postzygotic variant in ATP2C1., PMID:33569803

Generalized Hailey-Hailey disease: Novel splice-site mutations of ATP2C1 gene in Chinese population and a literature review., PMID:33345454

Novel ATP2C1 frame-shift mutation in a mild case of early onset sporadic Hailey-Hailey disease., PMID:33161602

A Novel Microduplication Spanning Exons 8-16 of ATP2C1 That Was Undetectable by Standard Sanger Sequencing in a Japanese Patient With Hailey-Hailey Disease., PMID:33015087

The Golgi Calcium ATPase Pump Plays an Essential Role in Adeno-associated Virus Trafficking and Transduction., PMID:32817219

Identification of ATP2C1 mutations in the patients of Hailey-Hailey disease., PMID:32487029

Novel missense mutation (A414P) in ATP2C1 in a case of familial Hailey-Hailey disease., PMID:32483844

Hailey-Hailey disease with a novel variant, c.1978dupG, in the ATP2C1 gene., PMID:32441372

Datasheet
$ 313
Product specifications
100 μg 313 1 mg 1629

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For research use only. Not for human or drug use.

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Recombinant Human ATP2C1 Protein, N-GST [YHF80501]
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