AGT2 (C4072T) SNP-Screen RT-PCR test, ready to use 0,2 ml tube format
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Catalog numberT01119-50-T
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Price:
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Size60 tests
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GroupPCR, polymerase chain reaction, RT-PCR mixes
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AboutTAQ or Pfu or Pfx or other enzymes are used for polycmerase chain reaction and have different specificity. The mores specific the lower the yield.
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PropertiesThermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR.
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Gene target
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Gene symbolAGXT2, TRT-AGT2-1, TRT-AGT2-2
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Short nameAGT2 (C4072T) SNP-Screen RT-PCR test, 2 tube format
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TechniqueRT-PCR, tube, PCR, The polymerase chain reaction (PCR) amplifies the DNA in your sample. For real time PCR the cycle threshold Ct values willneed to be set before the experiment. Than the RT-PCR starts from RNA and real time PCR quantitates the cDNA so the RNA in the sample on given time of the experiment. Sacace tubes
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Alternative nameAGT2 (C4072T) SNP-Screen Reverse transcription PCR test kit test, ready to use 0,2 milliliter tube supplied
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Alternative techniquertpcrkits, tests, tubes, dna-amplification
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Gene info
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Identity
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Gene
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Long gene namealanine--glyoxylate aminotransferase 2
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Synonyms gene name
- alanine-glyoxylate aminotransferase 2
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Synonyms
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Synonyms name
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GenBank acession
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Locus
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Discovery year2001-01-22
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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VEGA ID
Gene info
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Identity
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Gene
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Long gene nametRNA-Thr (anticodon AGT) 2-1
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Synonyms gene
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Synonyms gene name
- transfer RNA threonine 14 (anticodon AGU)
- transfer RNA-Thr (AGT) 2-1
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Synonyms
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GenBank acession
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Locus
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Discovery year2008-08-29
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Entrez gene record
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Classification
- Cytoplasmic transfer RNAs
Gene info
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Identity
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Gene
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Long gene nametRNA-Thr (anticodon AGT) 2-2
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Synonyms gene
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Synonyms gene name
- transfer RNA threonine 15 (anticodon AGU)
- transfer RNA-Thr (AGT) 2-2
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Synonyms
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GenBank acession
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Locus
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Discovery year2008-08-29
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Entrez gene record
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Classification
- Cytoplasmic transfer RNAs
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