T2040L,  Monarch RNA Cleanup Kit (50 µg) - 100 preps

T2040L, Monarch RNA Cleanup Kit (50 µg) - 100 preps

T2041L,  Monarch RNA Cleanup Binding Buffer - 80 ml

T2041L, Monarch RNA Cleanup Binding Buffer - 80 ml

T2040S, Monarch RNA Cleanup Kit (50 µg) - 10 preps

373,07 RON

The Monarch RNA Cleanup Kit (50 µg) enables fast and simple purification and concentration of up to 50 µg of RNA from enzymatic reactions.

SKU
NEB_T2040S

The Monarch RNA Cleanup Kit (50 µg) enables fast and simple purification and concentration of up to 50 µg of RNA from enzymatic reactions.

  • Ideal for cleanup and concentration of RNA after enzymatic treatments including DNase I, Proteinase K, labeling, capping or in vitro transcription (IVT)
  • Efficiently purify RNA ≥ 25 nt (a simple modification enables purification of RNA ≥ 15 nt)
  • Elute in ≥ 20 µl for concentrated RNA
  • 70-100% RNA recovery
  • Can be used to purify RNA from the aqueous phase following TRIzol® or similar extractions
  • Simplified workflow with a single wash buffer
  • Unique column design prevents buffer carryover and elution of silica particulates
  • Columns and buffers are available separately
  • Purified RNA is ready for use in a wide variety of downstream applications, including transfection

RNA Sample Type

Cleanup of previously purified RNA (TRIzol, phenol/ chloroform) and RNA from enzymatic reactions (in vitro transcription reactions, DNase I treatment)

Binding Capacity

50 µg

RNA Size Range

≥ 25 nt ( ≥ 15 nt with modified protocol)

Typical Recovery

70–100%

Elution Volume

20–50 µl

Purity

A260/280 > 1.8 and A260/230 > 1.8

Protocol Time

5 minutes of spin and incubation time

Compatible Downstream Applications

RT =-PCR, RNA library prep for NGS, Formation of ribonucleoprotein (RNP) complexes for genome editing studies, microinjection, RNA labeling, transfection

 

APPLICATIONS

RNA Cleanup and Concentration (including from the TRIzol aqueous phase)

RNA purified by other methods can be further purified

Enzymatic Reaction Cleanup

Enzymes such as RNA polymerases, DNase I, Proteinase K and phosphatases are removed allowing efficient desalting

In vitro Transcription Cleanup

Enzymes and excess NTPs are removed to yield highly pure synthesized RNA

RNA Gel Extraction

Purification of RNA from agarose gels

RNA Fractionation

Fractionation of RNA into small and large RNA pools

 

 

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Description

The Monarch RNA Cleanup Kit (50 µg) enables fast and simple purification and concentration of up to 50 µg of RNA from enzymatic reactions.

  • Ideal for cleanup and concentration of RNA after enzymatic treatments including DNase I, Proteinase K, labeling, capping or in vitro transcription (IVT)
  • Efficiently purify RNA ≥ 25 nt (a simple modification enables purification of RNA ≥ 15 nt)
  • Elute in ≥ 20 µl for concentrated RNA
  • 70-100% RNA recovery
  • Can be used to purify RNA from the aqueous phase following TRIzol® or similar extractions
  • Simplified workflow with a single wash buffer
  • Unique column design prevents buffer carryover and elution of silica particulates
  • Columns and buffers are available separately
  • Purified RNA is ready for use in a wide variety of downstream applications, including transfection

RNA Sample Type

Cleanup of previously purified RNA (TRIzol, phenol/ chloroform) and RNA from enzymatic reactions (in vitro transcription reactions, DNase I treatment)

Binding Capacity

50 µg

RNA Size Range

≥ 25 nt ( ≥ 15 nt with modified protocol)

Typical Recovery

70–100%

Elution Volume

20–50 µl

Purity

A260/280 > 1.8 and A260/230 > 1.8

Protocol Time

5 minutes of spin and incubation time

Compatible Downstream Applications

RT =-PCR, RNA library prep for NGS, Formation of ribonucleoprotein (RNP) complexes for genome editing studies, microinjection, RNA labeling, transfection

 

APPLICATIONS

RNA Cleanup and Concentration (including from the TRIzol aqueous phase)

RNA purified by other methods can be further purified

Enzymatic Reaction Cleanup

Enzymes such as RNA polymerases, DNase I, Proteinase K and phosphatases are removed allowing efficient desalting

In vitro Transcription Cleanup

Enzymes and excess NTPs are removed to yield highly pure synthesized RNA

RNA Gel Extraction

Purification of RNA from agarose gels

RNA Fractionation

Fractionation of RNA into small and large RNA pools