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D7656

Deoxyribonucleic acid, single stranded from salmon testes

For hybridization

Synonim(y):

single-stranded template DNA

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Wybierz wielkość

1 ML

230,00 zł

5 X 1 ML

1070,00 zł

230,00 zł


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Informacje o tej pozycji

Numer CAS:
UNSPSC Code:
41106310
eCl@ss:
32160414
NACRES:
NA.52
MDL number:
Assay:
9-11 mg/mL
Biological source:
fish testis
Form:
solution
Storage temp.:
−20°C

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biological source

fish testis

grade

Molecular Biology

assay

9-11 mg/mL

form

solution

concentration

10.0 ± 1.0 mg/mL in H2O

shipped in

dry ice

storage temp.

−20°C

Quality Level

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Ta pozycja
D915631149D8661
grade

for molecular biology

grade

for molecular biology

grade

for molecular biology, puriss. p.a.

grade

for molecular biology

Quality Level

200

Quality Level

200

Quality Level

-

Quality Level

200

form

solution

form

solution

form

lyophilized powder

form

solution

assay

9-11 mg/mL

assay

9-11 mg/mL (DNA concentration)

assay

-

assay

9-11 mg/mL (DNA concentration)

shipped in

dry ice

shipped in

dry ice

shipped in

-

shipped in

dry ice

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

General description

Deoxyribonucleic acid, single stranded from salmon testes is a ready-to-use solution of high quality, sonicated, single-stranded template DNA isolated from the testes of salmon.

Application

Deoxyribonucleic acid, single stranded from salmon testes has been used for/as:
  • in situ hybridization histochemistry of rat brain[1], human kidney sections[2] and renal biopsy tissues[3]
  • preparing standard curve of DNA[4]
  • prehybridization solution in southern and northern hybridizations[5]
  • dilution of the cDNA[6]
  • fluorescent in-situ hybridization (FISH)[7]
  • ChIP analysis[8]
  • a standard to analyse the degraded nucleosides of genomic DNA by high performance liquid chromatography[9]
  • a component of hybridization solution in FISH[10]
  • a control in DNA-DNA hybridization experiment between various bacterial species[11]
  • to precipitate probes in fluorescence in situ hybridization (FISH)[12][13][14]
For use as a blocking agent in Northern and Southern blotting.
Many factors contribute to the signal-to-noise ratio in nucleic acid hybridizations. These factors include the presence of solvent (formamide), hybridization temperature, length of hybridization, volume of hybridization solution, degree and method of agitation, use of blocking reagents, concentration and specific activity of the probe, use of molecular agents to increase the rate of nucleic acid reassociation, and the degree of stringency used during the washing of the membrane.

In order to decrease any non-specific hybridization of the probe to a substrate, blocking agents must be used. Generally, a combination of blocking reagent, detergent, and denatured, fragmented DNA is used to accomplish this. Sigma offers sonicated, denatured DNA from a variety of species for use as a blocking agent in Northern and Southern blotting and other nucleic acid hybridization techniques.
Suitable for use as a blocking agent in Southern hybridizations.

Preparation Note

This DNA is phenol-chloroform extracted, ethanol precipitated, and sonicated to produce single-stranded fragments which comigrate with the 587 and 831 base pair marker fragments.

Other Notes

DNA in solution will reanneal on standing at room temperature so it is recommended to boil the solution for 10 minutes and then cool on ice for at least 5 minutes prior to use.
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related product

Numer produktu
Opis
Cennik

Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Similar rates of chromosomal aberrant secondary oocytes in two indigenous cattle (Bos taurus) breeds as determined by dual-color FISH
Pauciullo, Alfredo, et al
Theriogenology, 675-683 (2012)
Frequency of aneuploidy in in vitro-matured MII oocytes and corresponding first polar bodies in two dairy cattle (Bos taurus) breeds as determined by dual-color fluorescent in situ hybridization
Nicodemo, D., et al
Theriogenology, 523-529 (2010)
Rune Thomsen et al.
PloS one, 8(8), e72110-e72110 (2013-08-31)
The intermediate filament network of astrocytes includes Glial fibrillary acidic protein (Gfap) as a major component. Gfap mRNA is alternatively spliced resulting in generation of different protein isoforms where Gfapα is the most predominant isoform. The Gfapδ isoform is expressed
D Suzuki et al.
Diabetes, 44(10), 1233-1238 (1995-10-01)
Increased mesangial expansion is one of the most characteristic histological changes in diabetic nephropathy (DN). Although the pathogenesis of DN remains unclear, recent studies associate interleukin (IL) 6 with mesangial proliferative glomerulonephritis. To elucidate the expression and localization of IL-6
XY aneuploidy rate in sperm of two ?minor? breeds of cattle (Bos taurus) by using dual color fluorescent in situ hybridization (FISH)
Pauciullo, Alfredo, et al
Theriogenology, 688-695 (2010)

Produkty

Dostępne procedury, odczynniki i sprzęt do fluorescencyjnej hybrydyzacji in situ (FISH).

Available Fluorescent in situ hybridization (FISH) procedures, reagents and equipment.

Powiązane treści

Questions

  1. What is the density of the deoxyribonucleic acid, single stranded from salmon testes, D7656?

    1 answer
    1. The density of the this product is not determined. The DNA concentration may range from 9.0 - 11.0 mg/mL. This value is lot-specific and reported in the Certificate of Analysis.

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