DNAH11 (NM_003777) Human 3' UTR Clone
CAT#: SC207762
3`UTR clone of dynein axonemal heavy chain 11 (DNAH11) for miRNA target validation
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Specifications
Product Data | |
Vector | pMirTarget |
Species | Human |
Transfection Reporter | RFP |
Assay Reporter | Luciferase |
E. coli Selection | Kanamycin (25 ug/mL) |
Mammalian Cell Selection | Neomycin |
Symbol | DNAH11 |
Synonyms | CILD7; DNAHBL; DNAHC11; DNHBL; DPL11 |
ACCN | NM_003777 |
Insert Size | 599 |
Sequence Data |
>SC207762 3'UTR clone of NM_003777
The sequence shown below is from the reference sequence of NM_003777. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GCAAAATGGGTTCTGGCTGGAGTGGCTCTGCTTCTAGAAGCGTAAGGTAACACTGGCATTCCTCTAGCCT CTGCTGGAGTGCAGTGAGGATTTTCTAGCATGTTGCTGCACTGTTCCCATGCACATTATTCTAACTTTTT AGTAACTCACACGTGCATTCTTTTTTCAACGCTATCCTTAGAGTGAAAGTCAGAAAAAAATACTAGAAAC TAACTCAGGGCTGAGCGTGGTGGCACACGACTGTAATCCCAGTTACTCAGGAGGTAGGAGAATCACTTGA ACCTAGGAGGCAAAGGTTGCAGTGAGCCGAGGTTGCACCACTGCACTCCCTCCTGGGCAACAGAACAAGA CTCCATCTCAAAAAAAAAAAAGTACATCATAAAAGTACATCATATGTGAACATGCAAAAGCAATGCAGCC GGAAAGAACGGAGATTTTAATTTTTAACAAACAACAAATTAAATTATTAGCCCTTAAACTCTTTCAAAAT ATAAAAGCAGCAGGCCCCAGGTGAGTCCTGAAGGAAGAGGCTAGCACTCTGTAAGGCCTCCAGTGTCCAG TGTCTACAATGTTGATGGTCCCCTTTTGTTCAGTCAAGT ACGCGTAAGCGGCCGCGGCATCTAGATTCGAAGAAAATGACCG |
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_003777.3 |
Summary | This gene encodes a ciliary outer dynein arm protein and is a member of the dynein heavy chain family. It is a microtubule-dependent motor ATPase and has been reported to be involved in the movement of respiratory cilia. Mutations in this gene have been implicated in causing Kartagener Syndrome (a combination of situs inversus totalis and Primary Ciliary Dyskinesia (PCD), also called Immotile Cilia Syndrome 1 (ICS1)) and male sterility. [provided by RefSeq, Mar 2013] |
Locus ID | 8701 |
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