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Key Documents

CRISPRPL02

Sigma-Aldrich

CRISPR GUS GAPDH Reporter Control for Dicots

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About This Item

Code UNSPSC :
12352200
Nomenclature NACRES :
NA.51

Produit recombinant

expressed in E. coli

Niveau de qualité

Conditionnement

vial of 50 μL

Concentration

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

Application(s)

CRISPR

selection

kanamycin

Conditions d'expédition

dry ice

Température de stockage

−20°C

Description générale

All-in-one, ready-to-use Cas9 and guide RNA (gRNA) expression plasmids with GUS Reporter

CRISPR Plant Cas9 products are intended for Agrobacterium-mediated plant transformation. The products are based on the type IIA CRISPR-Cas9 derived from Streptococcus pyogenes. The native Cas9 coding sequence is codon optimized for expression in monocots and dicots, respectively. The monocot Cas9 constructs contain a monocot U6 promoter for sgRNA expression, and the dicot Cas9 constructs contain a dicot U6 promoter.

Arabidopsis seedlings were germinated in 6 well tissue culture plates
The seedlings were infected with Agrobacterium which had the CRISPR plasmids with a GUS reporter. After 3-4 days of transfection the GUS expression was detected. b-glucuronidase (GUS) is an enzyme that hydrolyzes colorless glucuronides to yield colored product

Application

  • To verify successful integration of T-DNA in plant genome
  • GUS receptor wheat gGAPDH control for monocots for Agrobacterium mediated transformation

Caractéristiques et avantages

  • Low cost, genome editing option compared to other methods.
  • Easy to use
  • Online ordering
  • Ready to ship in 2 days

Composants

1 vial containing 50ul of 20ng/ul plasmid DNA
Keep reagent tubes closed when not in use.
Practice aseptic lab technique to avoid DNase contamination.

Principe

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.

Autres remarques

For ordering any of our custom CRISPR plant products please visit: CUSTOM ORDERING FORM

Informations légales

Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Protocoles

ZFNs and CRISPR/Cas9 advance targeted genome editing, opening new research avenues.

ZFNs and CRISPR/Cas9 advance targeted genome editing, opening new research avenues.

ZFNs and CRISPR/Cas9 advance targeted genome editing, opening new research avenues.

ZFNs and CRISPR/Cas9 advance targeted genome editing, opening new research avenues.

Contenu apparenté

Explore technology and reagent portfolios for plant breeding workflows, accelerating the development of new crop varieties.

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Explore technology and reagent portfolios for plant breeding workflows, accelerating the development of new crop varieties.

Explore technology and reagent portfolios for plant breeding workflows, accelerating the development of new crop varieties.

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