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Human GREM2 activation kit by CRISPRa

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SKU
GA112053
GREM2 CRISPRa kit - CRISPR gene activation of human gremlin 2, DAN family BMP antagonist
  $1,657.00
4 Weeks*

Frequently Bought Together (2)

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Specifications
Specifications
Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Target Symbol GREM2
Locus ID 64388
Components

GA112053G1, GREM2 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA112053G2, GREM2 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA112053G3, GREM2 gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077
OTI 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.
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Reference Data
RefSeq NM_022469
UniProt ID Q9H772
Synonyms CKTSF1B2; DAND3; PRDC
Summary This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted glycosylated protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. provided by RefSeq, Jul 2008
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Documents
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Other Versions
SKU Description Size Price
KN407388 GREM2 - KN2.0, Human gene knockout kit via CRISPR, non-homology mediated. 1 kit
$1,657.00

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*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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