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Recombinant Human ATP2C1 cell lysate

Cat.No. : ATP2C1-148HCL
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  • Gene Information
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Description : The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified.
Species : Human
Size : 100 ul
Storage Buffer : 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications : Western Blot;
Gene Name : ATP2C1 ATPase, Ca++ transporting, type 2C, member 1 [ Homo sapiens ]
Official Symbol : ATP2C1
Synonyms : ATP2C1; ATPase, Ca++ transporting, type 2C, member 1; BCPM, benign chronic pemphigus (Hailey Hailey disease); calcium-transporting ATPase type 2C member 1; ATP2C1A; KIAA1347; PMR1; secretory pathway Ca2+/Mn2+ ATPase 1; SPCA1; HUSSY-28; ATPase 2C1; ATPase, Ca(2+)-sequestering; ATP-dependent Ca(2+) pump PMR1; HHD; BCPM; hSPCA1;
Gene ID : 27032
mRNA Refseq : NM_001001485
Protein Refseq : NP_001001485
MIM : 604384
UniProt ID : P98194
Chromosome Location : 3q21.3
Pathway : Ion channel transport, organism-specific biosystem; Ion transport by P-type ATPases, organism-specific biosystem; Transmembrane transport of small molecules, organism-specific biosystem; calcium transport I, organism-specific biosystem;
Function : ATP binding; ATP binding; calcium ion binding; calcium-transporting ATPase activity; NOT calcium-transporting ATPase activity; calcium-transporting ATPase activity; calcium-transporting ATPase activity; hydrolase activity; hydrolase activity, acting on acid anhydrides, catalyzing transmembrane movement of substances; manganese ion binding; manganese-transporting ATPase activity; metal ion binding; nucleotide binding; signal transducer activity;

For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.


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Q&As (6)

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What factors regulate the expression of ATP2C1? 12/21/2022

The expression of ATP2C1 may be regulated by a variety of factors, including intracellular calcium levels, cell signaling pathways, transcription factors, and so on.

What is Hailey-Hailey disease? 10/15/2021

Hailey-Hailey disease is a rare genetic skin disease characterized by skin inflammation and lesions.

What is the role of ATP2Cin skin cells? 08/09/2021

It is a calcium transporter in skin cells and is responsible for the regulation of intracellular and extracellular calcium balance.

How do mutations in ATP2Ccause Hailey-Hailey disease? 07/03/2021

The mutation of ATP2C1 may lead to the dysfunction of ATP2C1 protein and affect the calcium homeostasis in skin cells, which may lead to Hailey-Hailey disease.

How is ATP2Ctranscription and translation regulated? 01/31/2020

The transcription and translation of ATP2C1 may be affected by various regulatory mechanisms such as chromatin alterations, activation of signaling pathways, and binding of transcription factors

What are the interactions of ATP2Cwith other proteins? 06/14/2019

ATP2C1 may interact with some proteins related to intracellular calcium signaling pathway to further regulate calcium transport and intracellular balance.

Customer Reviews (3)

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    ATP2C1n's repeatability is truly exceptional, consistently delivering reliable results even under challenging conditions.


      Since the purity of the protein was indeed excellent, there were no visible impurities or contaminants.


        ATP2C1 is ideal for Western-blot analysis, with strong bands and clear specificity.

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