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Safety Information

S1314

Sigma-Aldrich

Monoclonal Anti-SERCa2 ATPase antibody produced in mouse

clone 2A7-A1, ascites fluid

Synonym(s):

Anti-ATP2B, Anti-DAR, Anti-DD, Anti-SERCA2

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About This Item

MDL number:
MFCD00802883
UNSPSC Code:
12352203
NACRES:
NA.41

biological source

mouse

Quality Level

200

conjugate

unconjugated

antibody form

ascites fluid

antibody product type

primary antibodies

clone

2A7-A1, monoclonal

mol wt

antigen 110 kDa

contains

0.05% sodium azide

species reactivity

guinea pig, human, canine, mouse, rat, rabbit

technique(s)

immunoprecipitation (IP): suitable
western blot: suitable

UniProt accession no.

P16615

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... ATP2A2(488)
mouse ... Atp2a2(11938)
rat ... Atp2a2(29693)

General description

SERCa2 ATPase (sarco/endoplasmic reticulum calcium-ATPase 2) is also known as ATP2A2 (ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2). It codes for SERCA2a and SERCA2b, that are expressed in all tissues. SERCA2a is highly expressed in heart. SERCa2 is located on human chromosome 12q24.1.

Immunogen

canine cardiac sarcoplasmic reticulum vesicles

Application

Anti-SERCa2 ATPase antibody has been used in western blotting and immunocytochemistry.

Biochem/physiol Actions

Mutation of SERCa2 ATPase (sarco/endoplasmic reticulum calcium-ATPase 2) or ATP2A2 (ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2) causes Dyskeratosis follicularis. SERCA2a plays a major role in controlling cardiomyocyte Ca2+. ATP2A2 mutation may cause Darier disease (DD).

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Pricing

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

S1314-100UL-PW:
S1314-BULK:
S1314-VAR:
S1314-100UL:

Certificates of Analysis (COA)

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José Castellano et al.
Journal of molecular and cellular cardiology, 50(5), 894-902 (2011-02-23)
It is known that myocardium suffers serious alterations under ischemic conditions such as lipid overloading and electrophysiological alterations. However, it is unknown whether intracellular lipid accumulation and calcium dysfunction share common pathophysiological mechanisms under ischemia. The aims of this study
Humberto Muzi-Filho et al.
Physiological reports, 3(10) (2015-10-29)
Epidemiological and animal studies have shown that placental undernutrition impairs reproduction in adult offspring, but the underlying molecular mechanisms within the male genital tract remain unknown. Due to its special physiological characteristics in transport and the modulation of the environment
Daisuke Shimura et al.
American journal of physiology. Heart and circulatory physiology, 310(1), H92-103 (2015-11-01)
Sarcolipin (SLN) is a small proteolipid and a regulator of sarco(endo)plasmic reticulum Ca(2+)-ATPase. In heart tissue, SLN is exclusively expressed in the atrium. Previously, we inserted Cre recombinase into the endogenous SLN locus by homologous recombination and succeeded in generating
Modulation of sarcoplasmic reticulum Ca(2+)-ATPase by chronic and acute exposure to peroxynitrite
Gutierrez-Martin Y, et al.
European Journal of Biochemistry, 271(13), 2647-2657 (2004)
[Analysis of ATP2A2 gene mutations in a pedigree and a sporadic case with Darier disease]
Zhao X, et al.
Zhonghua yi xue yi chuan xue za zhi (Chinese Journal of Medical Genetics), 33(5), 641-644 (2016)
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