pCR-XL-TOPO-EFCAB4B
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Catalog numberPVT14138
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Price:
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Size2 ug
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GroupPCR, polymerase chain reaction
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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 symbolCRACR2A, BCL2L1, BCL11A
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Short namepCR-XL-TOPO-EFCAB4B
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TechniquePCR, 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.
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Alternative namePCR test kit-XL-TOPO-EFCAB4B
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Alternative techniquedna-amplification
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Gene info
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Identity
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Gene
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Long gene namecalcium release activated channel regulator 2A
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Synonyms gene
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Synonyms gene name
- EF-hand calcium binding domain 4B
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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 year2006-03-21
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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Classification
- EF-hand domain containing
Gene info
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Identity
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Gene
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Long gene nameBCL2 like 1
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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 year1997-10-30
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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Classification
- BCL2 family
- Protein phosphatase 1 regulatory subunits
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VEGA ID
Gene info
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Identity
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Gene
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Long gene nameBAF chromatin remodeling complex subunit BCL11A
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Synonyms gene
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Synonyms gene name
- ecotropic viral integration site 9
- B-cell CLL/lymphoma 11A (zinc finger protein)
- B cell CLL/lymphoma 11A
- BCL11A, BAF complex component
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Synonyms
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GenBank acession
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Locus
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Discovery year2001-02-28
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Entrez gene record
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Pubmed identfication
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RefSeq identity
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Classification
- Zinc fingers C2H2-type
- BAF complex
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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