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Merck
CN

A4140

Aequorin from jellyfish (Aequorea sp.)

Type III, solid

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UNSPSC Code:
12352202
MDL number:
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biological source

Aequorea sp.

type

Type III

form

solid

usage

 mg solid sufficient for ~200 calcium assays

composition

Protein, ~0.5% Bradford

application(s)

detection

storage temp.

−20°C

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General description

Apoaequorin has a mol. wt. approx. 22 kDa, and contains a molecule of coelenterazine hydroperoxide as the chromophoric prosthetic group. Upon binding Ca2+, aequorin decomposes to apoaequorin, coelenteramide, and CO2, and emits light.
Package sizes are based on total solids content

Biochem/physiol Actions

A bioluminescent protein; can be used to measure physiological levels of calcium in serum and subcellular organelles down to 10 μM.

Physical form

Contains buffer salts consisting mainly of sodium EDTA, pH 7.5

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

常规特殊物品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Denis Ottolini et al.
Methods in molecular biology (Clifton, N.J.), 937, 273-291 (2012-09-26)
In the last two decades the study of Ca(2+) homeostasis in living cells has been enhanced by the explosive development of genetically encoded Ca(2+)-indicators. The cloning of the Ca(2+)-sensitive photoprotein aequorin and of the green fluorescent protein (GFP) from the
Nazia Haq et al.
Assay and drug development technologies, 11(2), 93-100 (2012-10-11)
Gap junctions (GJs) are intercellular channels which are composed of the connexin family of proteins that allow electrical and chemical communications and synchronization in tissue ensembles. Evidence suggests that pharmaceutical modulators of these channels may have therapeutic potential or carry
Satoshi Inouye et al.
Protein expression and purification, 83(2), 205-210 (2012-04-28)
Highly purified histidine-tagged aequorin with a reactive cysteine residue (His-Cys4-aequorin) was obtained from the periplasmic space of Escherichia coli cells by nickel-chelate affinity chromatography and hydrophobic chromatography. The procedure yielded 40.3mg of His-Cys4-aequorin from 2L of cultured cells with over
Fen-Fen Lin et al.
The Journal of pharmacology and experimental therapeutics, 345(2), 225-238 (2013-03-12)
Calcium entry into T cells following antigen stimulation is crucial for nuclear factor of activated T cells (NFAT)-mediated T cell activation. The movement of calcium is mediated by calcium release-activated calcium (CRAC) channels. There are two key components of this
Daiana Minocci et al.
Biochimica et biophysica acta, 1833(7), 1632-1640 (2013-01-05)
Different optical imaging techniques have been developed to study neuronal activity with the goal of deciphering the neural code underlying neurophysiological functions. Because of several constraints inherent in these techniques as well as difficulties interpreting the results, the majority of

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