KIF21A Human Gene Knockout Kit (CRISPR)

CAT#: KN217610

KIF21A - human gene knockout kit via CRISPR

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 HDR-mediated knockout kit validation

USD 1,290.00


Availability*
4 Weeks

Size
    • 1 kit

Product images

Specifications

Product Data
Symbol KIF21A
Locus ID 55605
Kit Components

KN217610G1, KIF21A gRNA vector 1 in pCas-Guide vector

KN217610G2, KIF21A gRNA vector 2 in pCas-Guide vector

KN217610-D, donor DNA containing Left and right homologous arms and GFP-puro functional cassette.

GE100003, scramble sequence in pCas-Guide vector

Disclaimer 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 AK000059, NM_001173463, NM_001173464, NM_001173465, NM_017641, XM_005269007, XM_005269008, XM_005269009, XM_005269010, XM_005269011, XM_005269012, XM_005269013, XM_005269014, XM_006719493, XM_006719494, XM_011538556, XM_017019607, XM_017019608, XM_017019609, XM_017019610, XM_017019611, XM_040211, XM_040216
Synonyms CFEOM1; FEOM1; FEOM3A
Summary This gene encodes a member of the KIF4 subfamily of kinesin-like motor proteins. The encoded protein is characterized by an N-terminal motor domain a coiled-coil stalk domain and a C-terminal WD-40 repeat domain. This protein may be involved in microtubule dependent transport. Mutations in this gene are the cause of congenital fibrosis of extraocular muscles-1. Alternate splicing results in multiple transcript variants.[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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