HOXD4 (NM_014621) Human 3' UTR Clone
CAT#: SC203602
3' UTR clone of homeobox D4 (HOXD4) 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 | HOXD4 (NM_014621) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | HHO.C13; Hox-4.2; HOX-5.1; HOX4; HOX4B |
ACCN | NM_014621 |
Insert Size | 314 bp |
Sequence Data |
>SC203602 3’UTR clone of NM_014621
The sequence shown below is from the reference sequence of NM_014621. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC GACCACCACACGGACCTGACGACCTTATAGAAGTGGGGACCCTGGGCCCATCTCTCCCTGCGCACCAGG CTGAGCCGAAGCTGCGGGGGCAGGCCGGGCCTGCTGTCACCTCGCTGGGCTCTAAGGTACTGTGGGGTG GACCTGGGACAAGCAGGCCGCCCTCGGACTAGGTTAGCATCCTGCCCGAGGGCAGCCCCCTCCCTAGAG CGGGATGGGGATGGGAGGGGGGGCGGGATTCTCTCTCTAAGTATATTATATGGCAGGAGCTACTGAGAA CATAAAATCTTGGCGAGTCATTAAACTTATGAAAATCA 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_014621.3 |
Synonyms | HHO.C13; Hox-4.2; HOX-5.1; HOX4; HOX4B |
Summary | This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located at 2q31-2q37 chromosome regions. Deletions that removed the entire HOXD gene cluster or 5' end of this cluster have been associated with severe limb and genital abnormalities. The protein encoded by this gene may play a role in determining positional values in developing limb buds. Alternatively spliced variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008] |
Locus ID | 3233 |
MW | 11.5 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...