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D7656

Sigma-Aldrich

Deoxyribonucleic acid, single stranded from salmon testes

For hybridization

Synonym(s):

single-stranded template DNA

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
41106310
eCl@ss:
32160414
NACRES:
NA.52

grade

for molecular biology

Quality Level

Assay

9-11 mg/mL

form

solution

concentration

10.0 ± 1.0 mg/mL in H2O

shipped in

dry ice

storage temp.

−20°C

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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, human kidney sections and renal biopsy tissues
  • preparing standard curve of DNA
  • prehybridization solution in southern and northern hybridizations
  • dilution of the cDNA
  • fluorescent in-situ hybridization (FISH)
  • ChIP analysis
  • a standard to analyse the degraded nucleosides of genomic DNA by high performance liquid chromatography
  • a component of hybridization solution in FISH
  • a control in DNA-DNA hybridization experiment between various bacterial species
  • to precipitate probes in fluorescence in situ hybridization (FISH)
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.

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)
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
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)
Sydney Tang et al.
The Journal of clinical investigation, 111(4), 515-527 (2003-02-18)
Renal tubulointerstitial injury is characterized by inflammatory cell infiltrate; however, the stimuli for leukocyte recruitment are not fully understood. IL-8 is a potent chemokine produced by proximal tubular epithelial cells (PTECs). Whether nephrotic proteins stimulate tubular IL-8 expression remains unknown.

Articles

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

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