CLTCL1 (NM_001835) Human 3' UTR Clone
CAT#: SC207289
3' UTR clone of clathrin heavy chain-like 1 (CLTCL1) transcript variant 2 for miRNA target validation
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CNY 4,845.00
货期*
3周
规格
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经常一起买 (2)
Specifications
Product Data | |
Product Name | CLTCL1 (NM_001835) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CHC22; CLH22; CLTCL; CLTD |
ACCN | NM_001835 |
Insert Size | 547 bp |
Sequence Data |
>SC207289 3’UTR clone of NM_001835
The sequence shown below is from the reference sequence of NM_001835. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CTCGTGTTTGATTTTGATGGGCATGAATGAGACCCAGCTGATTGCACTAAGCCCTGCCGTGGGCCCAGC CCCTGCCAGCTTCCCCTATGGATATGCCTCTGCTCCCAACTTCGCCAGCCTCCAATGTACAACTTCCGC GTGTAGTGGGCGTTGTCACCACCCACCCTACCTGCAGAGTTACTAACTTCTCCAAGGAGCATGTCACTC CAGCAGCACAGGGGACGCAATGGGAGGCAGGGACACCTGGACAATATTTATTTTTGCTGAAACCCAATG ACGGCAACCTCTGAGCCATCCCAGAGCCTGGGGAGGCCAGGGTAGAGGCTGACGGCGCAAGACCAGCTT TAGCCGACAACAGAGACTGGACTGTGGGCCCTCCTGCTGGAGCCAGGCCTTCCTCCTGGGCGCCTCCGA CTGGCTGGAGCTGCCCCCTCCAGGCCAGTTTGAAGACTACATGAACACGTCTTGTTTGGAGGTACCGGA CCTCATAAAAGGACTCTCAGCCTCTTGGCAATCATAAATATTAAAGTCGGTTTATCCAGGCAAA 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_001835.4 |
Synonyms | CHC22; CLH22; CLTCL; CLTD |
Summary | This gene is a member of the clathrin heavy chain family and encodes a major protein of the polyhedral coat of coated pits and vesicles. Chromosomal aberrations involving this gene are associated with meningioma, DiGeorge syndrome, and velo-cardio-facial syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2009] |
Locus ID | 8218 |
MW | 20.1 |
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