BGC > Product Search > Proteinase K (from tritirachium album) | 39450-01-6

Hazard Symbols: Xn
WGKGermany: 1

MF	C29H27N2O12P
EINECS No.	254-457-8
Place of Origin	Shandong, China
Type	Agrochemical Intermediates, Dyestuff Intermediates, Flavor & Fragrance Intermediates, Syntheses Material Intermediates
Purity	99% Min
Brand Name	Unilong

Electrophoretic purity	≥ 95%
Enzyme activity	≥ 30U/mg
Nucleic acid residue	Invisible N.D
Deoxyribonuclease residue	Invisible N.D
Ribonuclease residue	Invisible N.D
20 microliter whole blood genomic DNA extraction from poultry DNA amount ≥ 5μ g

Description:
Proteinase K is a subtilisin-related serine protease. It was discovered from the fungus Engyodontium album. It can be used for removal of endogenous nucleases during the preparation of DNA and RNA, and for preparation of tissue sections for in situ hybridization. It is often used in pH range 7.5-9.0 and 37-70°C. Specific activity is ≥ 34 units/mg of protein.

• Molecular Weight:
• Boiling Point:831.1±75.0°C at 760 mmHg

Appearance:
Lyophilized Powder
Storage: Store at -20°C
Synonyms:
EC 3.4.21.64; endopeptidase K; Tritirachium alkaline proteinase; Tritirachium album serine proteinase; Tritirachium album proteinase K

Product Name: Proteinase K
CAS: 39450-01-6
MF: n.a.
MW: 0
EINECS: 254-457-8
storage temp. 2-8°C
Purity: 95 %
Package: 25kg/drum
Storage:Stored in a cool, ventilated warehouse. Keep away from fire and heat. Packing Seal. Should be oxidant, strong alkali separate storage, avoid mixing reservoir. Equipped with the appropriate variety and quantity of fire equipment. The storage area shall be provided with suitable material to contain the spill.


Uses :
Scientific research, experiment. Broad-spectrum protease, 95C heating 10 minutes, then completely inactivated. Can replace the DEPC treatment RNA extraction with the centrifuge tube and tip to achieve the purpose of inactivation RNase A, RNase-Free for the treatment of water. Full degradation of tissue or cell protein molecules, especially nucleic acids, in order to achieve the release and extraction of high-quality nucleic acid auxiliary reagents. For plasmid or genomic DNA, RNA isolation and protein blotting experiments.