Molecular Biology

RNA study


 

 

 

UptiDNAPure Total RNA Purification Kit - from animal tissues and cellular cultures

Applications

  • Total RNA Purification from animal tissues and cell cultures.

  • Purified RNA can be used in most downstream applications (reverse transcription-amplification, labeling, Northern blotting, etc.).

  • No phenolic extractions. Based on a modified Silica matrix, that binds RNA with a high specificity.

  • High integrity and purity of obtained RNA, without DNA contamination.

  • Fast and easy method: protocol completed in 35 minutes.

 

Description

Cat.#

Qty

UptiDNAPure Total RNA Purification Kit

from animal tissues and cellular cultures

UPS54671

25rxns

UPS54672

50rxns

--

UPS54673

100rxns

 

See also: Phenol, saturated

 

Quality control

Each lot is thoroughly tested to ensure maximum quality and lot to lot reproducibility. A total of 30 preparations are processed and used in a variety of downstream applications.

Store at 4şC or room temperature (depending on reagent).

Figure1.

Total RNA from 320 mg of rat liver obtained using UptiRNAPure Total RNA Purification Kit from animal tissues and cellular cultures.

RNA was eluted in a final volume of 100 µl. M: 100bp ladder Marker. Lane1: 1 µl of final eluate. Lane 2: 1/5 dilution of lane1. Lane 3: 1/5 dilution of lane 2.

 

Nucleotides

ATP, Na4

UP299232

25µmol

Adenosine-5’-triphosphate, tetrasodium salt, 100mM

CAS [987-65-5]

C10H12N5O14P3Na4

MW 595.15

Absorbance max. : 259 nm

e at absorbance max : 9,0 E x mmol-1 x cm-1

pH 7.0

Purity > 98 %

ATP is suitable for in vitro transcription and other in vitro assays. ATP is used as substrate for the reduction reaction to form the dATP. ATP is also used as energy source of enzymatic reactions.

CTP, Na4

UP314781

25µmol

Cytidine-5’-triphosphate, tetrasodium salt, 100mM

CAS [81012-87-5]

C9H12N3O13P3Na4

MW 571.13

Absorbance max. : 271 nm

e at absorbance max : 9,0 E x mmol-1 x cm-1

pH 7.0

Purity > 98 %

CTP is used as substrate for the reduction reaction to form dCTP.

CTP is suitable for in vitro RNA transcription.

NTP, Set

UP968680

4x25µmol

UP968681

4x25µmol

Ultrapure NTP Set, Nucleoside 5’-triphosphates, tetrasodium salts (100mM)

Purity > 98 %

Store at –20°C

NTPs are used as substrates for the reduction reaction to form dNTPs(1,2). NTPs are suitable for in vitro RNA transcription

Literature :

(1) Vitols, E., Blakley,R.L., J.Biol.Chem.,242,3035 (1967)

(2) Blakley, R.L, Methods in enzymology, Vol.II,246 (1978)

GTP, Na4

UP367852

25µmol

Guanosine-5’-triphosphate, tetrasodium salt, 100mM

CAS [36051-31-7]

C10H14N5O14P3Na4

MW 611.15

Absorbance max. : 253 nm

e at absorbance max : 9,0 E x mmol-1 x cm-1

pH 7.0

Purity > 98 %

GTP is used as substrate for the reduction reaction to form dGTP. GTP is RNAse free so is suitable for in vitro RNA transcription. GTP acts as coenzyme in the cell free protein synthesis.

UTP, Na4

UP23636A

25µmol

Uridine-5’-triphosphate, tetrasodium salt, 100mM

CAS [19817-92-6]

C9H11N2O15P3Na4

MW 572.10

Absorbance max. : 262 nm

e at absorbance max : 9,0 E x mmol-1 x cm-1

pH 7.0

Purity > 98 %

UTP is used as substrate for the reduction reaction to form dUTP.

UTP is suitable for in vitro RNA transcription.

Related Products

MOPS

UP06200

These buffer is commonly used for nucleotide solubilisation

 

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