H0268
Hexanucleotide Primers
lyophilized powder
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About This Item
NACRES:
NA.51
UNSPSC Code:
41106305
Form:
lyophilized powder
Storage temp.:
−20°C
Other Notes
1 A260 unit = approx. 20 μg
Hexanucleotide primers are a mixture of random 5′-hydroxyl hexanucleotides or hexamers, and can be used to quickly and efficiently prepare radioactive or non-radioactive probes using a DNA polymerase and a suitable DNA template.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
H0268-.2UN: + H0268-VAR: + H0268-BULK-N: + H0268-BULK: + H0268-1UN: + H0268-VAR-N:
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Bernhard Reuss et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 23(16), 6404-6412 (2003-07-25)
Multiple evidence suggests that fibroblast growth factors (FGFs), most prominently FGF-2, affect astroglial proliferation, maturation, and transition to a reactive phenotype in vitro, and after exogenous administration, in vivo. Whether this reflects a physiological role of endogenous FGF is unknown.
Sambrook, J., et al.
Molecular Cloning: A Laboratory Manual, 10-10 (1989)
Methods for non-radioactive labeling of nucleic acids.
Kessler, C. et al.
Nonisotopic Probing, Blotting, and Sequencing, 51-54 (1995)
A P Feinberg et al.
Analytical biochemistry, 132(1), 6-13 (1983-07-01)
A technique for conveniently radiolabeling DNA restriction endonuclease fragments to high specific activity is described. DNA fragments are purified from agarose gels directly by ethanol precipitation and are then denatured and labeled with the large fragment of DNA polymerase I
Juan J Ferreira et al.
The Journal of physiology, 597(1), 137-149 (2018-10-20)
At the end of pregnancy, the uterus transitions from a quiescent state to a highly contractile state. This transition requires that the uterine (myometrial) smooth muscle cells increase their excitability, although how this occurs is not fully understood. We identified
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