Human KAZALD1 activation kit by CRISPRa

CAT#: GA113097

KAZALD1 CRISPRa kit - CRISPR gene activation of human Kazal type serine peptidase inhibitor domain 1



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (2)
KAZALD1 Antibody - C-terminal region
    • 100 ul

CNY 5,250.00


KAZALD1 (Myc-DDK-tagged)-Human Kazal-type serine peptidase inhibitor domain 1 (KAZALD1)
    • 10 ug

CNY 2,400.00
CNY 3,990.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol KAZALD1
Locus ID 81621
Kit Components

GA113097G1, KAZALD1 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA113097G2, KAZALD1 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA113097G3, KAZALD1 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_001319303, NM_030929, NR_135067, NR_135068
Synonyms BONO1; FKSG28; FKSG40; IGFBP-rP10
Summary This gene encodes a secreted member of the insulin growth factor-binding protein (IGFBP) superfamily. The protein contains an insulin growth factor-binding domain in its N-terminal region, a Kazal-type serine protease inhibitor and follistatin-like domain in its central region, and an immunoglobulin-like domain in its C-terminal region. Studies of the mouse ortholog suggest that this protein may function in bone development and bone regeneration. This gene is hypomethylated and over-expressed in high-grade glioma compared to low-grade glioma, and thus the hypomethylated gene may be associated with cell proliferation and the shorter survival of patients with high-grade glioma. It is also one of numerous genes found to be deleted in a novel 5.54 Mb interstitial deletion, which is associated with multiple congenital anomalies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
*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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