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SpinPrep PCR Clean-up Kit

Rapid purification of PCR products for downstream procedures

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storage condition

OK to freeze

storage temp.


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


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2-D Clean-Up Kit Cytiva 80-6484-51


2-D Clean-Up Kit

storage condition

OK to freeze

storage condition

OK to freeze

storage condition


storage condition

room temperature (The wash buffer should be placed at -20 °C at least 1 h before use and may be s-red in a -20 °C freezer)

storage temp.


storage temp.


storage temp.


storage temp.


General description

Rapid purification of PCR products for downstream procedures
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


•82 mlSpinPrep Bind Buffer

•27 mlSpinPrep Wash Buffer

•10 mlSpinPrep Elute Buffer

•100SpinPrep Filters

•100Receiver Tubes

•100Eluate Receiver Tubes


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

Legal Information

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


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Hazard Classifications

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

Storage Class

10 - Combustible liquids



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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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