Human ST3GAL3 activation kit by CRISPRa

CAT#: GA104414

ST3GAL3 CRISPRa kit - CRISPR gene activation of human ST3 beta-galactoside alpha-2,3-sialyltransferase 3



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (2)
ST3GAL3 Rabbit polyclonal Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


ST3GAL3 (Myc-DDK-tagged)-Human ST3 beta-galactoside alpha-2,3-sialyltransferase 3 (ST3GAL3), transcript variant 10
    • 10 ug

CNY 5,488.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol ST3GAL3
Locus ID 6487
Kit Components

GA104414G1, ST3GAL3 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA104414G2, ST3GAL3 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA104414G3, ST3GAL3 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_001270459, NM_001270460, NM_001270461, NM_001270462, NM_001270463, NM_001270464, NM_001270465, NM_001270466, NM_006279, NM_174963, NM_174964, NM_174965, NM_174966, NM_174967, NM_174968, NM_174969, NM_174970, NM_174971, NM_174972, NR_073016, NR_073017, NR_073018, NR_073019, NR_073020, NR_073021, NR_073023, NM_001350619, NM_001350620, NM_001350621, NR_146867, NM_001363573
Synonyms EIEE15; MRT12; SIAT6; ST3GALII; ST3GalIII; ST3N
Summary The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with a form of autosomal recessive nonsymdromic cognitive disability as well as infantile epileptic encephalopathy. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2017]
*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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