APOE Leu48Pro SNP-Screen RT-PCR test, ready to use 0,2 ml tube format

• Catalog number
  T01148-50-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
  APOE   Leu48Pro   SNP-Screen   test   format  
• Gene symbol
  APOE
• Short name
  APOE Leu48Pro 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
  apolipoprotein E Leu48Pro 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
  apolipoprotein E, AD2 and LDLCQ5 and LPG, APOE and IDBG-56807 and ENSG00000130203 and 348, lipoprotein particle binding, nuclei, Apoe and IDBG-152108 and ENSMUSG00000002985 and 11816, APOE and IDBG-639311 and ENSBTAG00000010123 and 281004

Gene info

• Identity
  HGNC:613
• Gene
  APOE
• Long gene name
  apolipoprotein E
• Synonyms gene
  • AD2
• Synonyms gene name
  • Alzheimer disease 2 (APOE*E4-associated, late onset)
• GenBank acession
  • K00396
• Locus
  19q13.32
• Discovery year
  2001-06-22
• Entrez gene record
  348
• Pubmed identfication
  • 10662539
• RefSeq identity
  • NM_000041
• Classification
  • Apolipoproteins
• VEGA ID
  OTTHUMG00000128901
• Locus Specific Databases
  • ALSOD, the Amyotrophic Lateral Sclerosis Online Genetic Database

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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