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Merck
CN

70976

SpinPrep PCR Clean-up Kit

Rapid purification of PCR products for downstream procedures

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关于此项目

NACRES:
NA.52
UNSPSC Code:
41105500
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产品名称

SpinPrep PCR Clean-up Kit, Rapid purification of PCR products for downstream procedures

manufacturer/tradename

Novagen®

storage condition

OK to freeze

storage temp.

10-30°C

General description

The SpinPrep<TMSYMBOL></TMSYMBOL> PCR Clean-Up Kit is designedfor the rapid purification of DNA amplifiedin PCR. The 10-minute procedure involvesaddition of a binding buffer followed byadsorption of the DNA to a silica membrane ina spin column format. Following a wash step,the DNA is eluted in low-salt buffer. This kitremoves DNA polymerases, dNTPs, salts, and> 99% of primers so that they do not interferewith downstream applications such as cloning,sequencing, or labeling. PCR products from100 bp to > 12,000 bp can be cleaned up, withrecoveries of amplified DNA in the range of60-90% under standard conditions.
Column binding capacity: up to 6 g
PCR volume: 100 l/rxn
Typical recovery: 6090%
Size range: 100 bp to > 12,000 bp
Time required:< 10 min

Rapid purification of PCR products for downstream procedures

Other Notes

•82 mlSpinPrep Bind Buffer

•27 mlSpinPrep Wash Buffer

•10 mlSpinPrep Elute Buffer

•100SpinPrep Filters

•100Receiver Tubes

•100Eluate Receiver Tubes

Legal Information

NOVAGEN is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Multiple Toxicity Values, refer to MSDS (O)

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Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

存储类别

10 - Combustible liquids

wgk

WGK 1


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Yong H Park et al.
Investigative ophthalmology & visual science, 57(2), 508-526 (2016-02-13)
The α-amino-3-hydroxy-5-methyl-4-isoxazoleproprionic acid (AMPA) receptors (AMPAR) subunits can be posttranscriptionally modified by alternative splicing forming flip and flop isoforms. We determined if an ischemia-like insult to retinal ganglion cells (RGCs) increases AMPAR susceptibility to s-AMPA-mediated excitotoxicity through changes in posttranscriptional

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