ADRB2 (G46A) SNP-Screen RT-PCR test, ready to use 0,2 ml tube format

• Catalog number
  T01359-50-T
• Price
  Please ask
• Size
  60 tests

• Group
  PCR, polymerase chain reaction, RT-PCR mixes
• About
  TAQ or Pfu or Pfx or other enzymes are used for polycmerase chain reaction and have different specificity. The mores specific the lower the yield.
• Properties
  Thermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR.

• Gene target
  ADRB2   G46A   SNP-Screen   test   format  
• Gene symbol
  ADRB2
• Short name
  ADRB2 (G46A) SNP-Screen RT-PCR test, 2 tube format
• Technique
  RT-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
• Alternative name
  adrenoceptor b 2, surface (G46A) SNP-Screen Reverse transcription PCR test kit test, ready to use 0,2 milliliter tube supplied
• Alternative technique
  rtpcrkits, tests, tubes, dna-amplification
• Alternative to gene target
  adrenoceptor beta 2, surface, ADRB2R and ADRBR and B2AR and BAR and BETA2AR, ADRB2 and IDBG-52685 and ENSG00000169252 and 154, norepinephrine binding, nuclei, Adrb2 and IDBG-152615 and ENSMUSG00000045730 and 11555, ADRB2 and IDBG-648668 and ENSBTAG00000002144 and 281605

Gene info

• Identity
  HGNC:286
• Gene
  ADRB2
• Long gene name
  adrenoceptor beta 2
• Synonyms gene
  • ADRB2R
• Synonyms gene name
  • adrenergic, beta-2-, receptor, surface
  • adrenoceptor beta 2, surface
• Synonyms
  • ADRBR
  • BAR
  • B2AR
• GenBank acession
  • AF022953
• Locus
  5q32
• Discovery year
  1990-09-10
• Entrez gene record
  154
• RefSeq identity
  • NM_000024
• Classification
  • Adrenoceptors
• VEGA ID
  OTTHUMG00000129933

MeSH Data

• Name
  Polymerase Chain Reaction
• Concept
  Scope 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.
• Tree numbers
  • E05.393.620.500
• Qualifiers
  ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data

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