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Merck
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Key Documents

CRISPR02

Sigma-Aldrich

CRISPR Nickase EMX1 Positive Control

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About This Item

UNSPSC 코드:
41106609
NACRES:
NA.51

형태

liquid

Quality Level

포장

pkg of 3 vials (50μL aliquot for each of the 3 kit components)

농도

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

응용 분야

CRISPR

배송 상태

dry ice

저장 온도

−20°C

일반 설명

Validated CRISPR site, which serves as an experimental control for the Cas9-D10A Nickase system. A three component positive control system consisting of a CMV-driven Cas9-D10A Nickase plasmid, a U6-driven guide RNA plasmid targeting the sense strand of the human EMX1 gene and a U6-driven guide RNA plasmid targeting the antisense strand of the human EMX1 gene.

애플리케이션

Functional Genomics/Target Validation
  • Creation of gene knockouts in cell lines
  • Creation of knock-in cell lines with promoters, fusion tags or reporters integrated into endogenous genes

특징 및 장점

Serves as an experimental control for the CRISPR editing workflow using Cas9-D10A Nickase. Allows for validation of your system with the CRSIPR/Cas9 system. A positive result in a miss-match detection assay will indicate validation of your system.

성분

1 vial containing 1ug of a plasmid expressing the forward strand guide sequence. 1 vial containing 1ug of a plasmid expressing the reverse strand guide sequence. 1 vial containing 1ug of a plasmid expressing Cas9-D10A.

원리

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.

물리적 형태

Sigma U6-gRNA plasmid expressing a guide sequence to human EMX1 supplied at a concentration of 20ng/ul in 50ul. Sigma Cas9-D10A Nickase plasmid at a concentration of 20ng/ul in 50ul.

제조 메모

Sigma CRISPR plasmid products are delivered as mini-prep aliquots, which may not be suitable for transfection into particular cell types. For best results, we advise maxi-prepping plasmids using endotoxin-free DNA purification kits prior to transfection.

기타 정보

Typical transfection concentrations used in literature are in the ranges of >= 1.0ug/UL and <= 5uL of Cas9-D10A Nickase plasmids combined with >= 1.0ug/UL and <= 5uL of U6-gRNA plasmids. (All dosages above assume 0.5 to 1 million cells nucleofected)

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


시험 성적서(COA)

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문서 라이브러리 방문

문서

CRISPR endonucleases have shown wide variation in their activity, even among multiple CRISPRs designed within close genomic proximity.

자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..

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