KRT13 (NM_153490) Human 3' UTR Clone
CAT#: SC203573
3' UTR clone of keratin 13 (KRT13) transcript variant 1 for miRNA target validation
Need custom modification / cloning service?
Get a free quote
CNY 4,845.00
货期*
3周
规格
Product images
经常一起买 (2)
Specifications
Product Data | |
Product Name | KRT13 (NM_153490) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CK13; K13; WSN2 |
ACCN | NM_153490 |
Insert Size | 305 bp |
Sequence Data |
>SC203573 3’UTR clone of NM_153490
The sequence shown below is from the reference sequence of NM_153490. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGCCGCACTTCTGATGTCCGTAGGCCTTAAATCTGCCTGGCGTCCCCTCCCTCTGTCTTCAGCACCCAG AGGAGGAGAGAGCCGGCAGTTCCCTGCAGGAGAGAGGAGGGGCTGCTGGACCCAAGGCTCAGTCCCTCT GCTCTCAGGACCCCCTGTCCTGACTCTCTCCTGATGGTGGGCCCTCTGTGCTCTTCTCTTCCGGTCGGA TCTCTCTCCTCTCTGACCTGGATACGCTTTGGTTTCTCAACTTCTCTACCCCAAAGAAAAGATTATTCA ATAAAGTTTCCTGCCTTTCTGCAAACATA 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_153490.3 |
Synonyms | CK13; K13; WSN2 |
Summary | The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This type I cytokeratin is paired with keratin 4 and expressed in the suprabasal layers of non-cornified stratified epithelia. Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus. The type I cytokeratins are clustered in a region of chromosome 17q21.2. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been described. [provided by RefSeq, Jul 2008] |
Locus ID | 3860 |
MW | 11.3 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...