Sodium bicarbonate transporter like protein 11 (SLC4A11) Human Gene Knockout Kit (CRISPR)

CAT#: KN222743BN

SLC4A11 - human gene knockout kit via CRISPR, HDR mediated




 HDR-mediated knockout kit validation

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CNY 12,260.00


货期*
6周

规格
    • 1 kit

Product images

经常一起买 (3)
pCAS-Scramble, pCas-Guide vector with a scrambled sequence as a negative control (10 µg)
    • 10 ug

CNY 3,710.00


Goat Anti-SLC4A11 / BTR1 Antibody
    • 100 ug

CNY 5,371.00


SLC4A11 (tGFP-tagged) - Human solute carrier family 4, sodium borate transporter, member 11 (SLC4A11), transcript variant 1
    • 10 ug

CNY 11,680.00

Specifications

Product Data
Format 2 gRNA vectors, 1 mBFP-Neo donor, 1 scramble control
Donor DNA mBFP-Neo
Symbol Sodium bicarbonate transporter like protein 11
Locus ID 83959
Kit Components

KN222743G1, Sodium bicarbonate transporter like protein 11 gRNA vector 1 in pCas-Guide CRISPR vector

KN222743G2, Sodium bicarbonate transporter like protein 11 gRNA vector 2 in pCas-Guide CRISPR vector

KN222743BN-D, donor DNA containing left and right homologous arms and mBFP-Neo functional cassette.

GE100003, scramble sequence in pCas-Guide vector

Disclaimer These products are manufactured and supplied by OriGene under license from ERS. The kit is designed based on the best knowledge of CRISPR technology. The system has been functionally validated for knocking-in the cassette downstream the native promoter. The efficiency of the knock-out varies due to the nature of the biology and the complexity of the experimental process.
Reference Data
RefSeq NM_001174089, NM_001174090, NM_032034, NR_135000, NM_001363745
Synonyms BTR1; CDPD1; CHED2; dJ794I6.2; NABC1
Summary This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described. [provided by RefSeq, Mar 2010]
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

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