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Merck
CN

M4940

MMP Control-6

buffered aqueous solution

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UNSPSC Code:
12352203
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form

buffered aqueous solution

shipped in

dry ice

storage temp.

−20°C

General description

Concentrated, serum-free, cell culture media from human fibroblasts containing human matrilysin (MMP-7) as well as other MMPs and TIMPs.

Application

Used as a qualitative positive control in immunoblotting for MMP-7.

Physical form

Solution in 0.01 M phosphate buffered saline.

Analysis Note

MMP/TIMP Molecular weights:
MMP-No., Mr latent/active*
MMP-1, 52,000 / 43,000
MMP-2, 71,000 / 62,000
MMP-3, 52,000 / 43,000
MMP-7, 28,000 / 19,000
MMP-8, 51,000 / 42,000
MMP-9, 76,000 / 67,000
MMP-10, 52,000 / 44,000
MMP-11, 51,000 / 46,000
MMP-12, 52,000 / 20,000
MMP-13, 52,000 / 42,000
MMP-14, 64,000 / 54,000
MMP-15, 71,000 / 61,000
MMP-16, 66,000 / 56,000
MMP-17, 62,000 / 51,000
MMP-18, 53,000 / 42,000
*Mr is based on the cDNA sequence, excluding signal peptide. Some MMPs may have glycosylated forms of higher Mr . Thus, for example:
MMP-8 in neutrophils, but not other tissues, has Mr = 85,000 / 64,000.
MMP-9 has Mr = 92,000 / 84,000.
MMP-11 (stromelysin 3) has Mr = 64,000 / 46,000.
Human MMP-13 has a latent form of 65,000.
TIMP-1 has a molecular mass by sequencing of 20.6 kDa and a glycosylated mass of 28.5 kDa.
TIMP-2 has a molecular mass by sequencing of 21.5 kDa.
Matrix Metalloproteinases and TIMPS, Woessner, J.F., and Nagase, H., Oxford University Press (Oxford, UK: 2000) pp. 2 and 9.
Recommended use for immunoblotting: mix 1:1 with 2X SDS-PAGE buffer and apply 20-40 μl per lane.

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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Sung-Kyun Ko et al.
Nature chemistry, 6(10), 885-892 (2014-09-23)
Anion transporters based on small molecules have received attention as therapeutic agents because of their potential to disrupt cellular ion homeostasis. However, a direct correlation between a change in cellular chloride anion concentration and cytotoxicity has not been established for

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