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CAS9D10AMRNA

CRISPR Cas9-D10A Nickase mRNA

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팩 크기SKU재고 정보가격 (VAT 별도)
1 ea
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₩1,659,119

제품정보 (DICE 배송 시 비용 별도)

NACRES:
NA.51
UNSPSC Code:
12352200
Concentration:
500 ng/μL

₩1,659,119


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packaging

vial of 50 μL

Quality Level

concentration

500 ng/μL

application(s)

CRISPR

shipped in

dry ice

storage temp.

−70°C

General description

CRISPR Cas9-D10A Nickase mRNA generated through in-vitro transcription which has been capped and polyA-tailed. This mRNA should be used in conjunction with two purified guideRNAs. The use of RNA vs. plasmid constructs avoids complications with promoter-embryo compatibility as well as the possibility of random integration of nuclease and gRNA-expressing plasmids into the host animal genome.

Application

Functional Genomics/Transgenic Applications
  • Creation of gene knockouts in transgenic applications
  • Creation of knock-in animals with promoters, fusion tags or reporters integrated into endogenous genes

Biochem/physiol Actions

CRISPR/Cas systems are employed by bacteria and archaea as a defense against invading viruses and plasmids. Recently, the type II CRISPR/Cas system from the bacterium Streptococcus pyogenes has been engineered to function in eukaryotic systems using two molecular components: a single Cas9 protein and a non-coding guide RNA (gRNA). The Cas9 endonuclease can be programmed with a single gRNA, directing a DNA double-strand break (DSB) at a desired genomic location. Similar to DSBs induced by zinc finger nucleases (ZFNs), the cell then activates endogenous DNA repair processes, either non-homologous end joining (NHEJ) or homology-directed repair (HDR), to heal the targeted DSB.

Features and Benefits

RNA ready to use in transgenic applications. Must be used in conjunction with two purified guideRNA sequences to mediate a site specific doubel strand break in the DNA. Recent evidence indicates off-targeting by CRISPR endonucleases is a significant concern. To address this problem, Sigma has developed paired nickase technology to expand CRISPR DNA recognition tracts to lengths similar to those of ZFNs and TALENs.  Our experience suggests that paired nickases based on the Cas9-D10A mutant are most reliable. Our development work also suggests that the critical factor in producing active paired nickases is the positioning of gRNAs in a 5′-to-5′ orientation. For RNA based delivery of paired CRISPR nickases, we recommend the use of a three part system comprised of the Cas9-D10A mRNA and two T7 generated guideRNA sequences. To simplify the use of paired nickases, Sigma has on-line tools which allow access to a library of pre-designed paired nickases. Please check Sigma′s on-line CRISPR product offerings for the latest design sets.

Physical form

Sigma Cas9-D10A Nickase mRNA is supplied at concentrations of 500 ng/ul (50 ul Cas9-D10A mRNA, capped and polyA-tailed)

Preparation Note

While Sigma implements the same high quality RNA synthesis procedures that have been successful in many mRNA-based ZFN transgenic projects, we highly recommend centrifuging your final, concentration-adjusted CRISPR RNA samples immediately prior to microinjection to ensure all particulate material has been removed which may result in clogging of microinjection needles.

Other Notes

1 vial containing 25ug of Cas9-D10A Nickase mRNA.

Please note, product does not contain guideRNA sequence. This must be purchased separately through the Custom CRISPR product tab.
Must be used in conjunction with the RNA format of two guideRNA sequences in order to mediate a double strand break in the DNA.

While Sigma CRISPR RNA was not developed for robust application to cell culture, we have seen some success in detecting CEL-I activity using RNA-only formats for both CRISPR nucleases and paired nickases.  RNA-only delivery formats may be favorable for cell types which are sensitive to double stranded DNA such a dendritic cells or when promoter-cell incompatibilities exist.

Typical microinjection concentrations used in the literature are in the ranges of 20-200 ng/ul for Cas9-D10A Nickase mRNA and 10-50 ng/ul for gRNA.

유사한 품목 비교

전체 비교 보기

차이점 표시

1 of 1

이 품목
CAS9D10APCAS9NEOLVCAS9NEO
concentration

500 ng/μL

concentration

20 ng/μL in TE buffer; DNA (1μg of plasmid DNA)

concentration

20 ng/μL in TE buffer; DNA (1μg of plasmid DNA)

concentration

≥1 x 10 6 VP/ml virus (via p24 assay)

storage temp.

−70°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−70°C

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

shipped in

dry ice

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

packaging

vial of 50 μL

packaging

vial of 50 μL

packaging

vial of 50 μL

packaging

vial of 200 μL

application(s)

CRISPR

application(s)

CRISPR

application(s)

CRISPR

application(s)

CRISPR


저장 등급

12 - Non Combustible Liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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프로토콜

Learn about CRISPR Cas9, what it is and how it works. CRISPR is a new, affordable genome editing tool enabling access to genome editing for all.

관련 콘텐츠

Sigma-Aldrich® Advanced Genomics는 CRISPR, Cas9, 합성 가이드 RNA(sgRNA) 및 ZFN(Zinc Finger Nuclease)을 포함한 유전자 편집 및 침묵 기술의 선도적인 제공업체입니다.

Sigma-Aldrich® Advanced Genomics is the leading provider of gene editing and silencing technologies including CRISPR, Cas9, synthetic guide RNA (sgRNA), and Zinc Finger Nuclease (ZFN).





국제 무역 품목 번호

SKUGTIN
CAS9D10AMRNA-1EA04061833531495

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