ZBTB20 (NM_001164346) Human 3' UTR Clone

CAT#: SC211023

3' UTR clone of zinc finger and BTB domain containing 20 (ZBTB20) transcript variant 6 for miRNA target validation



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CNY 4,845.00


货期*
3周

规格
    • 10 ug

Product images

经常一起买 (2)
Firefly luciferase assay kit, 150 assays
    • 1 kit

CNY 1,520.00


DH5α Chemically Competent Cells (≥10^8 cfu/μg of pUC19 DNA)
    • 5 x 200 ul

CNY 1,280.00

Specifications

Product Data
Product Name ZBTB20 (NM_001164346) Human 3' UTR Clone
Vector pMirTarget
Synonyms DPZF; HOF; ODA-8S; PRIMS; ZNF288
ACCN NM_001164346
Insert Size 2000 bp
Sequence Data
>SC211023 3’UTR clone of NM_001164346
The sequence shown below is from the reference sequence of NM_001164346. The complete sequence of this clone may contain minor differences, such as SNPs.
Blue=Stop Codon Red=Cloning site

GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG
TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC
CACATGAGGATGCATGTGTCTGACGGATAAGTAGTATCTTTCTCTCTTTCTTATGAACAAAACAAAACA
ACAACAAAAAACAAACAAACAAAAAAGCTATGGCACTAGAATTTAAGAAATGTTTTGGTTTCATTTTTA
CTTTCTGTTTTTGTTTTTGTTTCGTTTCATTTTGTACTACATGAAGAACTGTTTTTTGCCTGCTGGTAC
ATTACATTTCCGGAGGCTTGGGTGAATAATAGTTTTCCCAGTCTCCCTCGGATGGTGGCCTTAAGGCCT
GGTAGTGCTTCAAGAGGTCCACTGGTTGGATCTCTAGCTACTGGCCTCTAAATACAACCCTTCTTTACA
AAAAAATCTTTTAAAAAAAAGTAAAAAAAAAAAAAAAATTTCCACTTGTGAAGAGCACTACAAAAAATA
TATAACAAAATCTAAAAGGCCTACTGTCTTTAAGTACACCGCTTGCAGTGTTTCAGTGGACATTTTCAC
AATTCTGGCCGCTTGGACTTCACAGTAACCAGTTAAAACTGTGGAATATCACTTCTGGTTGAAAACCCA
GAGGAAAGGCCCTGCTGTTTTCCACCTACCACGTTGTCTGATTTCATAAAAGGGCTGTGGGGGTGGGAA
GGGCAGTGGGTTCGGTGGTGTGGGAAAGAAAGACGAATGGCAGGCTTCTTCCCCAGATTCTGCCCGGGT
CCACACACCCTGGCCCACCTTCTCCATATCCCCCTCTTGCAGCAGAAGCCAGGAAGACTTGGACAAGCA
ACAAGCAACAGTGGCTATCGTATTTATTCAGTGTCTTCGCTGAGCCACAGCCTCAGCACAATCAAGAGG
GACTTTCATGAAAGGCAGGAATGCAGATAAAACAAAGATATCAGAAATTTGCACCTATGTTTCTAGGTA
CAAGAGAAGGATTATTTCCAACAATCTTTGCAAAAAAAAAAAAAGTGTCAGGATATATTCTTGTGGAAG
AGAAAAAGAAAAAGAAATGGAGGGTGGGGGGAACAATAAAAAGTTCTTGAGGCTTTTTTAATTCAAAAT
TTTATAGAGGGGCAAAAGTGACGTTTACCAGATAGAATGCTGATTTTTTTAATATATTTACAACAGTAT
TTGTGTAAAAAAAAAAACAAAAAAAGTGAAATTGTTAAAAGTAATTTTTTTCATTTTGGTTTTGCATAC
ACTGCCACCAATTCCTTCTCTTTTATTTTATTTCACACACATATATATATTTTTTGGTAAGTCAAGACT
GTTAAGGTTAGCGATACTGCTTCCAGATAGAAAGAATAAAAGGCAACTAAAGTTATATTTGAAAGAGAG
GAAGGATATTTTCTTCATATTTTTTTTAATTTTTCTTAATTTTTATTATTTTAAGTATTGCCTGGGTTG
ATGAGGGCCTCTGTGGCCAGCCCATCCCTGCTGTAATTTGAATTGCTGCTTTGTATTTTGATATGTAGT
TCTTTGACTTTAGCAAGCTTAAGTTGCCCCACTGAATAATTTTTTCAACTGATTCATCTAGAATTCTGT
TCTTTTTCATGGAAGAGACTTTATCTTTCAGAAAGAGATTGCTTGCTTCTCCAAAATTTCATTGAGATC
TTACAATTCTAGAATTTCTATTGACTTTACTTTTTTTCTTAGTGAAACACTAATAGTCTAGAAGTCTTG
ATAAATGGGGTCTTTTCTTTTGTGATCAGCCAGGAAGAGGAGTTCACAAAACTCTGCCATAGCTCCTCA
CCCTTCCCAACTACAAAGAGCATCATTATGAGAAGCCTGTTATAGATCAAGATGCATTGATGCCAAAAT
TACTTTTTTCCTTCCAAATATCACCTTCTGACTGTTTCCACCATGGTTAAGAGGGCTGAATAAGATGAT
CATTCTTTAGATGACGAATTAACCCTTGCTTCTTCGAAAGGTTTTAGGGAAATTAACAAAAAAATTCCC
AGATGCCAACAGCCACCATTCAAAAGACCACCAATCTATTGCATCATACCAGATGCCACTCTCTCTTC
ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCGACCAAGCGACGCCCAACCTGCCATCA
CGAGATTTCGATTCCACCGCCGCCTTCTATGAAAGG
Restriction Sites SgfI-MluI     
OTI Disclaimer Our molecular clone sequence data has been matched to the sequence identifier above as a point of reference. Note that the complete sequence of this clone is largely the same as the reference sequence but may contain minor differences , e.g., single nucleotide polymorphisms (SNPs).
Reference Data
RefSeq NM_001164346.2
Synonyms DPZF; HOF; ODA-8S; PRIMS; ZNF288
Summary This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]
Locus ID 26137
MW 78
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