C1orf2 (FAM189B) (NM_006589) Human 3' UTR Clone
CAT#: SC207896
3`UTR clone of family with sequence similarity 189 member B (FAM189B) transcript variant 1 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 | FAM189B |
Synonyms | C1orf2; COTE1 |
ACCN | NM_006589 |
Insert Size | 566 |
Sequence Data |
>SC207896 3'UTR clone of NM_006589
The sequence shown below is from the reference sequence of NM_006589. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC GGGAGACTGGGCTCTGACCTAGGCTTCTTGTCACACTGAACACATCCAGCCACAGGCACCAGCTGGTTGG GACCAGCAGCCCCCAGCATCCTCTTGCACTGGCTGGCACAAAAAGAAACCTGCTGTATACCCCCCAAAGT GTCCCTTTCCCTCCTACCTCTGGGGTCTCTTGCTGCTTGCCTCTGCTGCTCTGGACTGGGAGAGCTTCTG TCCTGTGCTGCATGGGTATTTAGACTGTGGGGGAGATGCCCCTTCTTATAGCACTGGAGGAGGAAAACAA ATTCTTGTCCCCCTCAGAATGAGAGTGGCTCTTTCTGATTTGCAAGGGCACTATGGTCAGGGCAAAGGCA TGGCCCAGGTGTTTAAGTACAGGGTGACGTGTGCCTATGCAATGGGGTGGTAAGGCAGGCACGAAGAGTC CAAAAAATCTAGGTGGCCTCTCAGCTCTGCCACCTCTAGCTGCATGACCTTGGGCAAGCTATGTAACCCC AATTGCCTGCTCCATTAAAGACTGTGAAGGTAGAATGTTTGTAAAGCTCTTAACAGTATGTAAGCCTTCA ATAAAT 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_006589.2 |
Summary | This gene is located near the gene for the lysosomal enzyme glucosylceramidase; a deficiency in this enzyme is associated with Gaucher disease. The encoded protein has been identified as a potential binding partner of a WW domain-containing protein which is involved in apoptosis and tumor suppression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010] |
Locus ID | 10712 |
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