IFT122 (NM_052990) Human 3' UTR Clone
CAT#: SC200860
3' UTR clone of intraflagellar transport 122 homolog (Chlamydomonas) (IFT122) transcript variant 4 for miRNA target validation
Need custom modification / cloning service?
Get a free quote
CNY 4845.00
货期*
3周
规格
Product images

推荐一起购买 (2)
Specifications
Product Data | |
Product Name | IFT122 (NM_052990) Human 3' UTR Clone |
Vector | pMirTarget |
Synonyms | CED; CED1; FAP80; SPG; WDR10; WDR10p; WDR140 |
ACCN | NM_052990 |
Insert Size | 272 bp |
Sequence Data |
>SC200860 3’UTR clone of NM_052990
The sequence shown below is from the reference sequence of NM_052990. The complete sequence of this clone may contain minor differences, such as SNPs. Blue=Stop Codon Red=Cloning site GGCAAGTTGGACGCCCGCAAGATCCGCGAGATTCTCATTAAGGCCAAGAAGGGCGGAAAGATCGCCGTG TAACAATTGGCAGAGCTCAGAATTCAAGCGATCGCC CGCAGGTGCAAGGATGACCCTGGCCCATGACCAGCATCCTGGGGACGGCCTGCACCCTCTGCCCGCCTT GGGGTCTGCTGGGCTGTGAAGGAGAATAAAGAGTTAAACTGTCAGAATGTGTTTCTTGCCCAGATGAAG TTTGTGTTTTGTGGGGGGGGCCTTGTGTAACCACGGAATTCCTATTTATGGCATTTCATGCCTTGTAAA TAGCACCAGGAGATGAGGAAGAGAATGTACATATATTTTCTAAGGAAAAAAATCTGTTACTTTCA 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_052990.3 |
Synonyms | CED; CED1; FAP80; SPG; WDR10; WDR10p; WDR140 |
Summary | This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This cytoplasmic protein contains seven WD repeats and an AF-2 domain which function by recruiting coregulatory molecules and in transcriptional activation. Mutations in this gene cause cranioectodermal dysplasia-1. A related pseudogene is located on chromosome 3. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013] |
Locus ID | 55764 |
MW | 10.7 |
Documents
Product Manuals |
FAQs |
Resources
Customer
Reviews
Loading...