RAIDD (CRADD) (NM_003805) Human 3' UTR Clone
CAT#: SC206690
3`UTR clone of CASP2 and RIPK1 domain containing adaptor with death domain (CRADD) 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 | CRADD |
Synonyms | MRT34; RAIDD |
ACCN | NM_003805 |
Insert Size | 501 |
Sequence Data |
>SC206690 3'UTR clone of NM_003805
The sequence shown below is from the reference sequence of NM_003805. The complete sequence of this clone may contain minor differences, such as SNPs. Red=Cloning site Blue=Stop Codon CAATTGGCAGAGCTCAGAATTCAAGCGATCGC TCCTGCACATGTTGGAGTGATGGTGCCTCCAGCAACCGCTGGGGAGTGTGTCCCTGAGTCATGTGGGCTG AATCCTGACTTTCACTCAGAGCAGGTGGTTTTTTGTGTAGGTTTGTTTTTTATTTTTGATGATCTTCAGA TGGAAGGAGAAAACAGGGTTTCCACTAGACATTACTTGAAAGGCCAGATTACTCAGCAGATCTCCCATGT TGGCTCAACAATTCTTTGTTTTTAATTGCTTGAAGATTGCATTGTTGTAATTGTTCAGTTTTTAAATGTG TAATGGCATTTTAATAGACTAGTAAATCACAGTGGTTCAAAATATATATCCATATATATATATATCCATA TATATATCTCATGTCATCACATTACAGGCAGGTGTCTCATATGTAAAACATTTACCTGAATGTTGTCTGA GGACTGAACTGTGGACTTTACTATTCATAATGATAAAATAATAAAATGCGAATTACTATATATAATGTGC CTCACTCATGA 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_003805.3 |
Summary | This gene encodes a protein containing a death domain (DD) motif. This protein recruits caspase 2/ICH1 to the cell death signal transduction complex, which includes tumor necrosis factor receptor 1 (TNFR1A) and RIPK1/RIP kinase, and acts in promoting apoptosis. A mutation in this gene was associated with cognitive disability. A related pseudogene is found on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
Locus ID | 8738 |
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