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Merck
CN

10821705001

Roche

DNA Molecular Weight Marker V

pkg of 50 μg (in 200 μl), solution

别名:

DNA Marker

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UNSPSC Code:
41105335
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form

solution

packaging

pkg of 50 μg (in 200 μl)

manufacturer/tradename

Roche

storage condition

avoid repeated freeze/thaw cycles

General description

Fragment mixture prepared by cleavage of pBR322 DNA with restriction endonuclease Hae III.

Size Range: 8 to 587 bp

Application

DNA Molecular Weight Marker V is used for the size determination of DNA in agarose gels. It simplifies accurate molecular weight determination of double-stranded DNA fragments generated by:

<UL><LI>Restriction digests</LI>

<LI>PCR</LI>

<LI>RT-PCR</LI></UL>

Preparation Note

Activator: Ammonia, pyridine, imidazole, all at pH >7; detergents

Working concentration: A suggested working ratio, for immediate use in coupling procedures, is 2 mg POD to 4 mg lgG (molar ratio = 2:1, POD:IgG).

Storage conditions (working solution): 2 to 8 °C
Once thawed we recommend further storage at 2 to 8 °C.
Store at -15–-25 °C. (until use)

Other Notes

50 μg = 1A260 unit
For life science research only. Not for use in diagnostic procedures.
Ready-to-use solution, 250μg/ml, in TE buffer (10mM Tris-HCl, 1mM EDTA, pH 8.0)
The mixture contains 22 DNA fragments with the following base pair lengths (1 base pair = 660 daltons): 8, 11, 18, 21, 51, 57, 64, 80, 89, 104, 123, 124, 184, 192, 213, 234, 267, 434, 458, 504, 540, and 587 as determined by computer analysis of the pBR322 sequence.
Note: Fragment lengths are derived from computer analysis of the DNA sequence. Depending on the size range of the marker, the smallest fragments will only be visible on overloaded gels.

存储类别

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

does not flash

flash_point_c

does not flash

法规信息

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分析证书(COA)

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Julia Romero et al.
Nature protocols, 3(11), 1729-1735 (2008-10-18)
The lamin B2 locus is the only mammalian origin whose replication initiation points (RIPs) have been mapped. Although this paper was published 8 years ago, no further mammalian RIP-mapping studies have been reported, largely due to technical difficulties of ligation-mediated

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