Human SLC26A5 activation kit by CRISPRa

CAT#: GA117826

SLC26A5 CRISPRa kit - CRISPR gene activation of human solute carrier family 26 member 5



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
Rabbit Polyclonal Anti-SLC26A5 Antibody
    • 100 ul

CNY 5,250.00


SLC26A5 (Myc-DDK-tagged)-Human solute carrier family 26, member 5 (prestin) (SLC26A5), transcript variant a
    • 10 ug

CNY 5,448.00
CNY 5,800.00


Rabbit Polyclonal Anti-SLC26A5 Antibody
    • 25 ul

CNY 800.00
CNY 1,280.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol SLC26A5
Locus ID 375611
Kit Components

GA117826G1, SLC26A5 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA117826G2, SLC26A5 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA117826G3, SLC26A5 gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Disclaimer These products are manufactured and supplied by OriGene under license from ERS. The kit is designed based on the best knowledge of CRISPRa SAM technology. The efficiency of the activation can be affected by many factors, including nucleosome occupancy status, chromatin structure and the gene expression level of the target, etc.
Reference Data
RefSeq NM_001167962, NM_001321787, NM_198999, NM_206883, NM_206884, NM_206885, NR_120441, NR_120442, NR_120443, NR_135801, NR_135802
Synonyms DFNB61; PRES
Summary This gene encodes a member of the SLC26A/SulP transporter family. The protein functions as a molecular motor in motile outer hair cells (OHCs) of the cochlea, inducing changes in cell length that act to amplify sound levels. The transmembrane protein is an incomplete anion transporter, and does not allow anions to cross the cell membrane but instead undergoes a conformational change in response to changes in intracellular Cl- levels that results in a change in cell length. The protein functions at microsecond rates, which is several orders of magnitude faster than conventional molecular motor proteins. Mutations in this gene are potential candidates for causing neurosensory deafness. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Nov 2009]
*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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