CRISPRPL02

CRISPR GUS GAPDH Reporter Control for Dicots

Manufacturer: Sigma Aldrich

Select a Size

Pack Size SKU Availability Price
1 EA CRISPRPL02-1-EA In Stock ₹ 39,944.25

CRISPRPL02 - 1 EA

₹ 39,944.25

In Stock

Quantity

1

Base Price: ₹ 39,944.25

GST (18%): ₹ 7,189.965

Total Price: ₹ 47,134.215

recombinant

expressed in E. coli

Quality Level

200

packaging

vial of 50 μL

concentration

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

application(s)

CRISPR

selection

kanamycin

shipped in

dry ice

storage temp.

−20°C

Related Products

Img

Sigma Aldrich

CRISPRPL01

--

Img

Sigma Aldrich

DCAS9P300

--

Img

Sigma Aldrich

CAS9D10AP

--

Img

Sigma Aldrich

DCAS9P300RFP

--

Img

Sigma Aldrich

DCAS9P300VP

--

Img

Sigma Aldrich

ESPCAS9BST

--

Img

Sigma Aldrich

CAS9P

--

Img

Sigma Aldrich

FNCAS9P

--

Description

  • General description: All-in-one, ready-to-use Cas9 and guide RNA (gRNA) expression plasmids with GUS ReporterCRISPR 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
  • Features and Benefits: Low cost, genome editing option compared to other methods.Easy to useOnline orderingReady to ship in 2 days
  • Components: 1 vial containing 50ul of 20ng/ul plasmid DNAKeep reagent tubes closed when not in use. Practice aseptic lab technique to avoid DNase contamination.
  • Principle: 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.
  • Other Notes: For ordering any of our custom CRISPR plant products please visit: CUSTOM ORDERING FORM
  • Legal Information: CRISPR Use License Agreement

SAFETY INFORMATION

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Compare Similar Items

Show Difference

Img

Sigma Aldrich

CRISPRPL02

--


recombinant:
expressed in E. coli

Quality Level:
200

packaging:
vial of 50 μL

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

application(s):
CRISPR

selection:
kanamycin

shipped in:
dry ice

storage temp.:
−20°C

Img

CritiCore Protective Wear

CRITAPPLOGO

--


recombinant:
__

Quality Level:
__

packaging:
__

concentration:
__

application(s):
__

selection:
__

shipped in:
__

storage temp.:
__

Img

Millipore

CRK101006

pore size 0.1 μm, cartridge nominal...


recombinant:
__

Quality Level:
400

packaging:
__

concentration:
__

application(s):
__

selection:
__

shipped in:
__

storage temp.:
__

Img

Millipore

CRK102006

pore size 0.1 μm, cartridge nominal...


recombinant:
__

Quality Level:
400

packaging:
__

concentration:
__

application(s):
__

selection:
__

shipped in:
__

storage temp.:
__