pCR4-TOPO-SMAD9 Plasmid
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Catalog numberPVT16040
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Price348.4 USD
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Size2 ug
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KitPlasmid mini made and maxi DNA purification kits can be silica gel or anion exchange, endotoxin free and are used to produce pure plasmids that are small DNA molecules within a cell separated from chromosomal DNA and can replicate independently. They are most commonly found in bacteria as small circular, double-stranded DNA molecules; however, plasmids are sometimes present in archaea and eukaryotic organisms. In nature, plasmids often carry genes that may benefit the survival of the organism, for example antibiotic resistance. While the chromosomes are big and contain all the essential information for living, plasmids usually are very small and contain only additional information. Artificial plasmids are widely used as vectors in molecular cloning, serving to drive the replication of recombinant DNA sequences within host organisms.
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Gene target
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Gene symbolSMAD9-IT1, SMAD9
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Short namepCR4-TOPO-SMAD9 Plasmid
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Techniqueplasmid, plasmids in 1
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Alternative namepCR4-TOPO-SMAD family member 9 Plasmid
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Alternative techniqueplasmids
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Alternative to gene targetSMAD family member 9, MADH6 and MADH9 and PPH2 and SMAD8 and SMAD8A and SMAD8B, SMAD9 and IDBG-24637 and ENSG00000120693 and 4093, transforming growth factor beta receptor, nuclei, Smad9 and IDBG-144967 and ENSMUSG00000027796 and 55994, BT.61870 and IDBG-629870 and ENSBTAG00000007589 and 540806
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Gene info
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Identity
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Gene
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Long gene nameSMAD9 intronic transcript 1
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Synonyms gene
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Synonyms gene name
- SMAD9 antisense RNA 1 (non-protein coding)
- SMAD9 antisense RNA 1
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Locus
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Discovery year2011-04-18
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Classification
- Intronic transcripts
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VEGA ID
Gene info
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Identity
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Gene
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Long gene nameSMAD family member 9
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Synonyms gene
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Synonyms gene name
- MAD, mothers against decapentaplegic homolog 9 (Drosophila)
- SMAD, mothers against DPP homolog 9 (Drosophila)
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Synonyms
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Locus
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Discovery year1997-07-25
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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Classification
- SMAD family
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VEGA ID
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Locus Specific Databases
MeSH Data
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Name
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ConceptScope note: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
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Tree numbers
- E05.393.620.500
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Qualifiersethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data