MC3T3-E1 Subclone 14-CAS9

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MC3T3-E1 Subclone 14-CAS9

MC3T3-E1 Subclone 14-CAS9 Order

Catalog#YC-C026-Cas9-H

Price (USD)-

Size 1*10^6

Instruction

MC3T3-E1 Subclone 14 Cell Line was generated by CRISPR-U™ gene-editing technology to stably express Cas9 protein.

Cell Info

Catalog YC-C026-Cas9-H
Cell line MC3T3-E1 Subclone 14-CAS9 Cell Type Mouse Anterior Parietal Bone Cell Line
Morphology Epithelial-like, adherent Passage ratio 1:3~1:5
Culture method 90% Alpha MEM+10%FBS
Cryopreservation solution 50%Alpha MEM+40%FBS+10%DMSO
Special Note

Product Validation Data

RT-QPCR
Sample NameTarget NameCт MeanΔCт
MC3T3-E1 Subclone 14-CAS9Cas921.014574055.88625145
MC3T3-E1 Subclone 14-CAS9h-actin-B15.12832260
MC3T3-E1 Subclone 14Cas933.4172821018.85072040
MC3T3-E1 Subclone 14h-actin-B14.56656170
Cutting Efficiency Validation
Note: The above figure shows the sequencing peaks of the MC3T3-E1 Subclone 14-CAS9 stable cell pool which is electroporated by Inpp5k gene targeting gRNA plasmid, after 48h antibiotic screening. The red arrow indicates the position where the nested peak appears, which shows that the genotype of the target site is significantly changed due to the cutting. Therefore, it indicates that Cas9 nuclease is successfully expressed.

Product Advantage

  • (1)Easy to use:Cas9 cell lines in our cell bank can stably express Cas9 protein. Each Cas9 Stable Cell Line is easy to use and enables gene knockout simply by transfecting gRNA, while transfection of gRNA and donor DNA results in gene knock-in or point mutations
  • (2)High-efficient KO:These Cas9 stable cell lines have been used to construct the KO cell lines for various genes, gene KO efficiency 5-10 times improved.
  • (3)High-quality cell:Selected cells, low passages, good cell condition, high activity, applicable for all kinds of gene-editing experiments.
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