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DATP-RO

Roche

dATP

99% (dNTP), <0.9% (dNDP), solution, 100 mM

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Synonym(s):
2′-Deoxyadenosine 5′-triphosphate sodium salt solution, dATP

description

PCR Grade, sodium salt

Quality Level

Assay

99% (dNTP)

form

solution

usage

sufficient for 125,000 standard reactions (03732681001)
sufficient for 31,250 standard reactions (11969013001)
sufficient for 6,250 standard reactions (11934511001)

packaging

pkg of 1,250 μL (11969013001 [100 mM])
pkg of 4 × 1,250 μL (03732681001 [4x100 mM])
pkg of 250 μL (11934511001 [100 mM])

manufacturer/tradename

Roche

concentration

<0.9% (dNDP)
100 mM

storage temp.

−20°C

SMILES string

[Na+].Nc1ncnc2n(cnc12)[C@H]3C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OP(O)([O-])=O)O3

InChI

1S/C10H16N5O12P3.Na/c11-9-8-10(13-3-12-9)15(4-14-8)7-1-5(16)6(25-7)2-24-29(20,21)27-30(22,23)26-28(17,18)19;/h3-7,16H,1-2H2,(H,20,21)(H,22,23)(H2,11,12,13)(H2,17,18,19);/q;+1/p-1/t5-,6+,7+;/m0./s1

InChI key

YJWCICGGRLOGEH-VWZUFWLJSA-M

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This Item
11051440001D6920DNSTP-RO
dATP 99% (dNTP), &lt;0.9% (dNDP), solution, 100&#160;mM

Roche

DATP-RO

dATP

dATP =98%, solution, 100&#160;mM, suitable for DNA sequencing, suitable for DNA amplification

Roche

11051440001

dATP

form

solution

form

solution

form

liquid

form

-

packaging

pkg of 1,250 μL (11969013001 [100 mM]), pkg of 4 × 1,250 μL (03732681001 [4x100 mM]), pkg of 250 μL (11934511001 [100 mM])

packaging

pkg of 250 μL (25 μmol; 100 mM)

packaging

-

packaging

pkg of 4 × 100 μL (11277049001 [4x10 μmol]), pkg of 40 × 100 μL (11922505001 [40x100mM])

manufacturer/tradename

Roche

manufacturer/tradename

Roche

manufacturer/tradename

-

manufacturer/tradename

Roche

concentration

<0.9% (dNDP), 100 mM

concentration

100 mM

concentration

10 mM

concentration

-

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

General description

2′-Deoxyadenosine 5′-triphosphate (dATP) is made up of a nucleobase attached to deoxyribose and a 5′-hydroxyl on the sugar bound to a chain of three phosphate residues. dATP is used by cells for synthesis of DNA by DNA polymerases.
dATP, PCR Grade, is a 100 mM clear colorless solution of the sodium salt (pH 8.3). PCR Grade nucleotides from Roche are specially manufactured and purified to the highest possible chemical purity. PCR Grade nucleotides contain at least 99% of the relevant deoxynucleoside-triphosphate (dNTP) and less than 0.9% deoxynucleoside-diphosphate (dNDP).

Application

2′-Deoxyadenosine 5′-triphosphate sodium salt solution is used in DNA sysnthesis reactions such as PCR, DNA sequencing and molecular cloning techniques.
Quality
Function tested in RT-PCR. Tested for absence of contaminating deoxyribonucleases, ribonucleases and nicking activities according to the current Quality Control procedures.
dATP, PCR Grade, is suitable for many applications where high-quality reagents are required. Such procedures include reverse transcription (RT), polymerase chain reaction (PCR), RT-PCR, DNA labeling reactions, and sequencing/cycle sequencing analysis.

Physical form

solution of dATP in water (pH 8.3).

Preparation Note

Working solution: We recommend to prepare a deoxynucleotide mix containing dATP, dCTP, dGTP, dTTP (10 mM, each); (e.g., for the preparation of 100 μl nucleotide mix add 10 μl of dATP, dCTP, dGTP, dTTP (each) to 60 μl Water, PCR Grade).

Other Notes

For general laboratory use.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

does not flash

Flash Point(C)

does not flash


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Danos C Christodoulou et al.
Current protocols in molecular biology, Chapter 4, Unit4-Unit4 (2011-04-08)
RNA-seq is a method for studying the transcriptome of cells or tissues by massively parallel sequencing of tens of millions of short DNA fragments. However, the broad dynamic range of gene expression levels, which span more than five orders of
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Diagnostic molecular pathology : the American journal of surgical pathology, part B, 13(3), 144-150 (2004-08-24)
RNA extraction still relies almost exclusively on the use of fresh or frozen tissue, limiting the number of samples that can be analyzed, and there is a growing need for means of global mRNA analysis of archived formalin-fixed paraffin-embedded tissue

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