추천 제품
생물학적 소스
bovine
Quality Level
재조합
expressed in Pichia pastoris
형태
lyophilized powder
특이 활성도
≥4,000 units/mg protein
분자량
~39 kDa
기술
DNA extraction: suitable
solubility
H2O: soluble (pH 4.0-9.0)
적합성
suitable for molecular biology
응용 분야
diagnostic assay manufacturing
외래 활성
RNAse and protease, free
저장 온도
2-8°C
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애플리케이션
Deoxyribonuclease I bovine has been used in a study to investigate the inhibition of DNA polymerase by extracts of rat liver. Deoxyribonuclease I bovine has also been used in a study to investigate the effects of ionic strength on enzymic activity.
Deoxyribonuclease I bovine has been used in the preparation of cold cell lysis buffer, complete RNA lysis buffer, cell lysis buffer for testing the expression of recombinant tagged protein.
The enzyme from Sigma has been used for the digestion of DNA extracted from Agave spp. clones. The enzyme was used during a study that investigated the effect of epigenetic changes on the regulatory expression of KNOTTED1-like HOMEOBOX (KNOX) transcription factors.
Used for the removal of DNA from protein samples.
생화학적/생리학적 작용
DNase I is an endonuclease that acts on phosphodiester bonds adjacent to pyrimidines to produce polynucleotides with terminal 5′-phosphates. The pH optimum is found to be between 7 and 8. Divalent cations such as Mn2+, Ca2+, Co2+, and Zn2+ are activators of the enzyme. A concentration of 5 mM Ca2+ stabilizes the enzyme against proteolytic digestion. 2-Mercaptoethanol, chelators, sodium dodecyl sulfate (SDS) and actin are known to inhibit the enzyme activity.
Digests single- and double-stranded DNA to a mixture of mono- and oligonucleotides carrying 5′ phosphates and 3′ OH termini. This catalytic activity is divalent ion-dependent. In the presence of Mg2+, DNase I hydrolyzes each strand of double-stranded DNA randomly and independently. In the presence of Mn2+, both strands can be cleaved.
특징 및 장점
- RNA purification by removing DNA
- Prepare DNA for nick translation1
- Footprinting assays to determine DNA-protein interactions2
단위 정의
One unit will produce a ΔA260 of 0.001 per min per mL reaction mixture using calf thymus DNA at pH 5.0 and 25°C
물리적 형태
supplied as a lyophilized powder containing glycine as a stabilizer
제조 메모
Produced without using any animal cells or animal derived materials.
The enzyme powder may be reconstituted in water or any buffer at pH 4.0-9.0, except phosphate buffer. Calcium chelators should be avoided. 10 mg/mL solution of DNAse I in 0.15 M NaCl may lose <10% of its activity when stored for a week in aliquots at –20 °C. The same solutions stored in aliquots at 2-8 °C can lose approximately 20% activity. It remains active for upto five hours at 60 °C and loses activity in <10 minutes at 68 °C. It loses activity at the rate of 6%/hour in acetate buffer (pH 5.0) and tris buffer ((pH 7.2) at 1 mg/mL concentration.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Protein expression and purification, 97, 29-36 (2014-03-04)
The genome of the psychrophilic fish-pathogen Aliivibrio salmonicida encodes a putative ATP-dependent DNA ligase in addition to a housekeeping NAD-dependent enzyme. In order to study the structure and activity of the ATP dependent ligase in vitro we have undertaken its
Quantitative proteomics of breast tumors: Tissue quality assessment to clinical biomarkers.
Proteomics, 17(6), 1600335-1600335 (2017)
Recombinant expression and purification of an ATP-dependent DNA ligase from Aliivibrio salmonicida.
Protein Expression and Purification, 97(4), 29-36 (2014)
Genome-scale CRISPR-Cas9 knockout and transcriptional activation screening.
Nature Protocols, 12(4), 828-828 (2017)
Properties of chromatographically purified bovine pancreatic deoxyribonuclease.
The Journal of biological chemistry, 244(3), 917-923 (1969-02-10)
문서
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