Recombinant Human ATP2C2 Protein (Met1-Tyr106), N-GST-tagged

Cat.No. : ATP2C2-0123H
Product Overview : Recombinant human ATP2C2 (Met1-Tyr106) was fused with the N-GST tag and was expressed in E. coli.
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Source : E. coli
Species : Human
Tag : N-GST
Form : Lyophilized powder/frozen liquid
Molecular Mass : 38.92 kDa
Protein Length : Met1-Tyr106
Purity : >90% as determined by SDS-PAGE
Notes : For research use only.
Storage : Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8 centigrade for one week. Store at -20 to -80 centigrade for twelve months from the date of receipt.
Storage Buffer : 0.01M PBS, pH 7.4, 0.02% NLS
Reconstitution : Reconstitute in sterile water for a stock solution.
Shipping : They are shipped out with dry ice/blue ice unless customers require otherwise.
Gene Name : ATP2C2 ATPase, Ca++ transporting, type 2C, member 2 [ Homo sapiens (human) ]
Official Symbol : ATP2C2
Synonyms : AT2C2_HUMAN; ATP2C2; ATPase 2C2; ATPase, Ca++ transporting, type 2C, member 2; Calcium-transporting ATPase type 2C member 2; DKFZp686H22230; KIAA0703; Secretory pathway Ca(2+)-ATPase 2; ATP2C2; SPCA2
Gene ID : 9914
mRNA Refseq : NM_014861
Protein Refseq : NP_055676
MIM : 613082
UniProt ID : O75185

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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Customer Reviews (3)

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    Since the protein has a short half-life, it is more potent and less likely to cause side effects compared to other similar proteins.


      Protein manufacturers consistently produce products of the highest quality with a firm commitment to purity, potency, and consistency.


        ATP2C2 manufacturer's commitment to environmental sustainability is evident in its production processes, using green and renewable resources.

        Q&As (6)

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        What is the link between ATP2C2 and cardiovascular disease? 04/11/2022

        ATP2C2 maintains calcium homeostasis in cardiomyocytes, and mutation of ATP2C2 may lead to abnormal myocardial systolic function, which in turn is associated with cardiovascular diseases such as myocardial infarction.

        In what physiological processes does ATP2C2 function? 03/01/2022

        ATP2C2 plays a role in physiological processes such as intracellular regulation of calcium ion concentration, cytoskeletal assembly, neurotransmitter release, muscle contraction, and cell proliferation.

        How do mutations in ATP2C2 cause neurological diseases? 01/12/2022

        Mutation of ATP2C2 may lead to the dysfunction of ATP2C2, and then affect the intracellular calcium balance, neurotransmitter release and other key processes in the nervous system, leading to the occurrence of nervous system diseases.

        What diseases may be caused by ATP2C22 mutations? 11/17/2021

        Mutations in ATP2C2 may be associated with neurological diseases such as Alzheimer's disease, cardiovascular diseases such as myocardial infarction, metabolic disorders, and cancer.

        Does ATP2C2 have a potential therapeutic role? 12/19/2019

        Given the important role of ATP2C2 in multiple physiological processes, studying its disease-related mutations and calcium regulation mechanism may provide new clues and directions for the treatment of related diseases.

        What is the specific role of ATP2C2 in neurotransmitter release? 05/23/2019

        This is responsible for the transport and regulation of intracellular calcium ions during neurotransmitter release, ensuring that neurotransmitters can be released correctly into the synaptic cleft.

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