Human TCF4 activation kit by CRISPRa

CAT#: GA104778

TCF4 CRISPRa kit - CRISPR gene activation of human transcription factor 4



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CN¥ 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
Rabbit Polyclonal Anti-TCF4 Antibody
    • 50 ug

CN¥ 4,628.00


TCF4 (Myc-DDK-tagged)-Human transcription factor 4 (TCF4), transcript variant 1
    • 10 ug

CN¥ 7,368.00


TCF4 Rabbit polyclonal Antibody
    • 100 ul

CN¥ 3,280.00

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Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol TCF4
Locus ID 6925
Kit Components

GA104778G1, TCF4 gRNA vector 1 in pCas-Guide-GFP-CRISPRa, Target Sequence: GCTGAGATAGCATCCTGAAA

GA104778G2, TCF4 gRNA vector 2 in pCas-Guide-GFP-CRISPRa, Target Sequence: AGACTCTTCCAGCTTTGCCA

GA104778G3, TCF4 gRNA vector 3 in pCas-Guide-GFP-CRISPRa, Target Sequence: ATGCTGCACAAGTGTTACCA

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Reference Data
RefSeq NM_001083962, NM_001243226, NM_001243227, NM_001243228, NM_001243230, NM_001243231, NM_001243232, NM_001243233, NM_001243234, NM_001243235, NM_001243236, NM_003199, NM_001306207, NM_001306208, NM_001330604, NM_001330605, NM_001348211, NM_001348212, NM_001348213, NM_001348214, NM_001348215, NM_001348216, NM_001348217, NM_001348218, NM_001348219, NM_001348220, NM_001369567, NM_001369571, NM_001369574, NM_001369577, NM_001369579, NM_001369580, NM_001369581, NM_001369585, NM_001369586, NM_001369568, NM_001369569, NM_001369570, NM_001369572, NM_001369573, NM_001369575, NM_001369576, NM_001369578, NM_001369582, NM_001369583, NM_001369584
Synonyms bHLHb19; E2-2; ITF-2; ITF2; PTHS; SEF-2; SEF2; SEF2-1; SEF2-1A; SEF2-1B; SEF2-1D; TCF-4
Summary This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Jul 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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