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Merck
CN

S1439

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

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
Conjugate:
unconjugated
Clone:
IID8, monoclonal
Application:
ICC, IF, IHC (f), WB
Citations:
12
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conjugate

unconjugated

Quality Level

antibody form

purified from hybridoma cell culture

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

10 - Combustible liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

常规特殊物品
低风险生物材料

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Related Content

Instructions


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
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
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



Global Trade Item Number

SKUGTIN
S1439-100UL04061837813825