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The GenCRISPR™
Ultra eSpCas9 product line provides customers with a selection of research use,
basic GMP and GMP compliant Cas9 nucleases. The Cas9 protein can be formed with
the guide RNA into a ribonucleoprotien (RNP) complex. The use of an RNP complex
to perform gene editing has been shown to reduce the challenges encountered
with other CRISPR gene editing techniques such as viral and plasmid delivery.
Challenges include off-target effects, cell viability and transcription/translational
challenges.

GenCRISPR™ Ultra eSpCas9-N-NLS
Research, tag-free is a mutant form of Cas9
nuclease and is produced by expression in an E. coli strain carrying a plasmid encoding the eSpCas9 gene from Streptococcus pyogenes with an N-terminal
nuclear localization signal (N-NLS). GenCRISPR™ Ultra eSpCas9-N-NLS Research,
tag-free delivers higher fidelity
and less off-target activity than wild-type SpCas9 nuclease.

The GenCRISPR™
Ultra eSpCas9 product line provides customers with a selection of research use,
basic GMP and GMP compliant Cas9 nucleases. The Cas9 protein can be formed with
the guide RNA into a ribonucleoprotien (RNP) complex. The use of an RNP complex
to perform gene editing has been shown to reduce the challenges encountered
with other CRISPR gene editing techniques such as viral and plasmid delivery.
Challenges include off-target effects, cell viability and transcription/translational
challenges.

GenCRISPR™ Ultra eSpCas9-N-NLS
Research, tag-free is a mutant form of Cas9
nuclease and is produced by expression in an E. coli strain carrying a plasmid encoding the eSpCas9 gene from Streptococcus pyogenes with an N-terminal
nuclear localization signal (N-NLS). GenCRISPR™ Ultra eSpCas9-N-NLS Research,
tag-free delivers higher fidelity
and less off-target activity than wild-type SpCas9 nuclease.

The GenCRISPR™
Ultra eSpCas9 product line provides customers with a selection of research use,
basic GMP and GMP compliant Cas9 nucleases. The Cas9 protein can be formed with
the guide RNA into a ribonucleoprotien (RNP) complex. The use of an RNP complex
to perform gene editing has been shown to reduce the challenges encountered
with other CRISPR gene editing techniques such as viral and plasmid delivery.
Challenges include off-target effects, cell viability and transcription/translational
challenges.

GenCRISPR™ Ultra eSpCas9-N-NLS
Research, tag-free is a mutant form of Cas9
nuclease and is produced by expression in an E. coli strain carrying a plasmid encoding the eSpCas9 gene from Streptococcus pyogenes with an N-terminal
nuclear localization signal (N-NLS). GenCRISPR™ Ultra eSpCas9-N-NLS Research,
tag-free delivers higher fidelity
and less off-target activity than wild-type SpCas9 nuclease.

GenCRISPR™ Ultra NLS-Cas9-basic GMP is utilized for CRISPR gene editing applications. The Cas9 nuclease forms a stable ribonucleoprotein (RNP) complex with the guide RNA (gRNA) component. With the help of nuclear localization signal (NLS) expressed with the Cas9 nuclease, the RNP complex enters the nucleus and cleaves the target gene. When compared with a plasmid-based delivery system, the RNP delivery system has been observed to increase the on-target gene editing efficiency and decrease off-target effects.

GenCRISPR™ Ultra NLS-Cas9-basic GMP is utilized for CRISPR gene editing applications. The Cas9 nuclease forms a stable ribonucleoprotein (RNP) complex with the guide RNA (gRNA) component. With the help of nuclear localization signal (NLS) expressed with the Cas9 nuclease, the RNP complex enters the nucleus and cleaves the target gene. When compared with a plasmid-based delivery system, the RNP delivery system has been observed to increase the on-target gene editing efficiency and decrease off-target effects.

GenCRISPR™ Ultra NLS-Cas9-basic GMP is utilized for CRISPR gene editing applications. The Cas9 nuclease forms a stable ribonucleoprotein (RNP) complex with the guide RNA (gRNA) component. With the help of nuclear localization signal (NLS) expressed with the Cas9 nuclease, the RNP complex enters the nucleus and cleaves the target gene. When compared with a plasmid-based delivery system, the RNP delivery system has been observed to increase the on-target gene editing efficiency and decrease off-target effects.

GenCRISPR™ Ultra NLS-Cas9-GMP is utilized for CRISPR gene editing applications. It is manufactured in compliance with ISO 13485 and GMP quality management system standards and with stringent process controls and complete documentation records. This product is a ideal choice for most CRISPR gene editing applications where high editing efficiency is preferred.

GenCRISPR™ Ultra NLS-Cas9-GMP is utilized for CRISPR gene editing applications. It is manufactured in compliance with ISO 13485 and GMP quality management system standards and with stringent process controls and complete documentation records. This product is a ideal choice for most CRISPR gene editing applications where high editing efficiency is preferred.

The
GenCRISPR™ Ultra Cas9 product line provides customers with a selection of
research use, GMP preclinical and GMP compliant Cas9 nucleases. The Cas9
protein can be formed with the guide RNA into a ribonucleoprotien (RNP)
complex. The use of an RNP complex to perform gene editing has been shown to
reduce the challenges encountered with other CRISPR gene editing techniques
such as viral and plasmid delivery. Challenges include off-target effects, cell
viability and trascprition/translational challenges.

GenCRISPR™ Ultra Cas9 is
produced by expression in an E. coli
strain carrying a plasmid encoding the Cas9 gene from Streptococcus pyogenes with an N-terminal nuclear localization
signal (NLS).

The
GenCRISPR™ Ultra Cas9 product line provides customers with a selection of
research use, GMP preclinical and GMP compliant Cas9 nucleases. The Cas9
protein can be formed with the guide RNA into a ribonucleoprotien (RNP)
complex. The use of an RNP complex to perform gene editing has been shown to
reduce the challenges encountered with other CRISPR gene editing techniques
such as viral and plasmid delivery. Challenges include off-target effects, cell
viability and trascprition/translational challenges.

GenCRISPR™ Ultra Cas9 is
produced by expression in an E. coli
strain carrying a plasmid encoding the Cas9 gene from Streptococcus pyogenes with an N-terminal nuclear localization
signal (NLS).

The
GenCRISPR™ Ultra Cas9 product line provides customers with a selection of
research use, GMP preclinical and GMP compliant Cas9 nucleases. The Cas9
protein can be formed with the guide RNA into a ribonucleoprotien (RNP)
complex. The use of an RNP complex to perform gene editing has been shown to
reduce the challenges encountered with other CRISPR gene editing techniques
such as viral and plasmid delivery. Challenges include off-target effects, cell
viability and trascprition/translational challenges.

GenCRISPR™ Ultra Cas9 is
produced by expression in an E. coli
strain carrying a plasmid encoding the Cas9 gene from Streptococcus pyogenes with an N-terminal nuclear localization
signal (NLS).

Molecular Formula : C19 H22 N4 O3

Molecular Formula : C19 H22 N4 O3

Molecular Formula : C19 H22 N4 O3

Wash solution for use with GENECLEAN SPIN Glassmilk.

GENECLEAN SPIN NEW WASH

• Designed to optimally purify DNA fragments from 100 bp to 300 kb. No carryover of matrix into DNA solution is found.
• Works with either centrifuge or vacuum system.

• Designed to optimally purify DNA fragments from 100 bp to 300 kb. No carryover of matrix into DNA solution is found.
• Works with either centrifuge or vacuum system.

Aaqueous suspension of proprietary silica matrix that has been treated so that it can be easily resuspended by hand.

For isolation of up to 20 μg DNA from bones, preserved tissues, soil organisms, and animal by-products.

For the rapid purification of DNA from TAE and TBE agarose gels. Optimal purification of 200 bp to 20 kb DNA. Each spin column can bind up to 10 μg of DNA. Kit can also be used to purify DNA from polyacrylamide gels

For the rapid purification of DNA from TAE and TBE agarose gels. Optimal purification of 200 bp to 20 kb DNA. Each spin column can bind up to 10 μg of DNA. Kit can also be used to purify DNA from polyacrylamide gels

For the rapid purification of DNA from TAE and TBE agarose gels. Optimal purification of 200 bp to 20 kb DNA. Each spin column can bind up to 10 μg of DNA. Kit can also be used to purify DNA from polyacrylamide gels

Prepared aqueous suspension of proprietary silica matrix that contains TBE Modifier so it can be used with TAE- or TBE-buffered agarose gels.

Prepared aqueous suspension of proprietary silica matrix that contains TBE Modifier so it can be used with TAE- or TBE-buffered agarose gels.

Prepared aqueous suspension of proprietary silica matrix that contains TBE Modifier so it can be used with TAE- or TBE-buffered agarose gels.

For the rapid purification of DNA fragments of 200 bp – 300 kb from solutions and agarose gels using spin columns.

For the rapid purification of DNA fragments of 200 bp – 300 kb from solutions and agarose gels using spin columns.

For the rapid purification of DNA fragments of 200 bp – 300 kb from solutions and agarose gels using spin columns.

Optimized for the purification of 0.1 – 10 kb PCR fragments.

Optimized for the purification of 0.1 – 10 kb PCR fragments.

Optimized for the purification of 0.1 – 10 kb PCR fragments.

Aqueous solution of guanidine chaotropic binding salt optimized for the purification of genomic sized DNA.

GENECLEAN® Turbo GNomic Salt Solution

Aqueous solution of guanidine chaotropic binding salt optimized for the purification of genomic sized DNA.

Flexible kit designed for the purification of DNA fragments of sizes 0.1 – 300 kb from TAE or TBE buffered agarose gels, PCR reactions and other enzymatic solutions.

Flexible kit designed for the purification of DNA fragments of 0.1 – 300 kb from TAE or TBE buffered agarose gels, PCR reactions and other enzymatic solutions.

For the purification of DNA fragments of 0.1 – 300 kb from TAE or TBE buffered agarose gels, PCR reactions or solutions. No ethanol precipitation required. Rapid spin of vacuum based process

Flexible kit designed for the purification of DNA fragments of sizes 0.1 – 300 kb from TAE or TBE buffered agarose gels, PCR reactions and other enzymatic solutions.

GENECLEAN® Turbo Salt Solution

Molecular Formula : C20 H40 N4 O10 . 2 H2 O4 S

Molecular Formula : C20 H40 N4 O10 . 2 H2 O4 S

Molecular Formula : C29 D3 H28 N7 O

Molecular Formula : C29 D3 H28 N7 O

Genipin

Genipin

Geniposide

Geniposide

Molecular Formula : C17 H24 O10

Molecular Formula : C17 H24 O10