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S1439

Sigma-Aldrich

Monoclonal Anti-SERCa2 ATPase antibody produced in mouse

clone IID8

Synonym(s):

Monoclonal Anti-Sarcoplasmic or Endoplasmic Reticulum Ca2+ ATPase

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About This Item

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

antibody form

purified from hybridoma cell culture

Quality Level

antibody product type

primary antibodies

clone

IID8, monoclonal

species reactivity

bovine, canine, rat, human, pig, rabbit

technique(s)

immunocytochemistry: suitable
immunohistochemistry (frozen sections): 1:500
indirect immunofluorescence: suitable
western blot: 1:500-1:5,000

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

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

Immunogen

purified canine cardiac sarcoplasmic reticulum.

Physical form

Supplied as a solution in PBS containing 0.05% sodium azide.

Other Notes

Not suitable for immunoblotting in rat SERCA2.

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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Storage Class Code

10 - Combustible liquids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Ning Li et al.
Traffic (Copenhagen, Denmark), 18(4), 232-241 (2017-02-06)
Darier's disease (DD) is an autosomal dominantly inherited skin disorder caused by mutations in sarco/endoplasmic reticulum Ca2+ -ATPase 2 (SERCA2), a Ca2+ pump that transports Ca2+ from the cytosol to the endoplasmic reticulum (ER). Loss of desmosomes and keratinocyte cohesion
Mirella Telles Salgueiro Barboni et al.
Progress in retinal and eye research, 95, 101137-101137 (2022-11-21)
Duchenne muscular dystrophy (DMD) is caused by X-linked inherited or de novo DMD gene mutations predominantly affecting males who develop early-onset muscle degeneration, severely affecting their quality of life and leading to reduced life expectancy. DMD patients may also develop
Karolina Varga et al.
Cell calcium, 55(2), 78-92 (2014-01-21)
The expression of the plasma membrane Ca2+ ATPase (PMCA) isoforms is altered in several types of cancer cells suggesting that they are involved in cancer progression. In this study we induced differentiation of MCF-7 breast cancer cells by histone deacetylase
Victor Galvan-Alvarez et al.
Redox biology, 66, 102859-102859 (2023-09-05)
When high-intensity exercise is performed until exhaustion a "functional reserve" (FR) or capacity to produce power at the same level or higher than reached at exhaustion exists at task failure, which could be related to reactive oxygen and nitrogen species
Luca Hegedũs et al.
International journal of cancer, 140(12), 2758-2770 (2016-11-05)
Oncogenic mutations of BRAF lead to constitutive ERK activity that supports melanoma cell growth and survival. While Ca2+ signaling is a well-known regulator of tumor progression, the crosstalk between Ca2+ signaling and the Ras-BRAF-MEK-ERK pathway is much less explored. Here

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