HEV I, II, III& IV Real Time RT-PCR Kit

  • Catalog number
    HR-0305-02
  • Price
    Please ask
  • Size
    25tests/kit
  • Product type
    Hepatitis Virus
  • Instrument 1
    Ⅲ, Ⅳ
  • Instrument 2
    (Ⅲ) PE5700, MJ-Opticon & other single color systems, (Ⅳ) ABI7000, ABI7300, ABI7500, ABI7900, ABI StepOne, StepOne plus, MJ-Opticon2, MJ-chromo4, MX3000P, MX3005P, Smart Cycler II, Rotor-Gene 6000, LightCycler 480, CFX 96, iCycler iQ4, iCycler iQ5 & other multi-color systems
  • Nucleic Acid
    RNA
  • Note
    NA
  • 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
    HEV   III   Real   Time   Kit  
  • Gene symbol
    CPLX3, MGAT3, MGST3, IL33, P4HA3, CASP5, THAP4, IGHVIII-82, MT-CSB3, IGHVIII-67-4
  • Short name
    HEV I, II, III& IV Real Time RT-PCR Kit
  • Technique
    RT-PCR, 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.
  • Alternative name
    HEV I, II, III& IV Real Time Reverse transcription PCR test kit reagent
  • Alternative technique
    rtpcrkits, kits, dna-amplification
  • Alternative to gene target
    v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog, C-Kit and CD117 and PBT and SCFR, KIT and IDBG-18980 and ENSG00000157404 and 3815, transferase activity, Extracellular, Kit and IDBG-172083 and ENSMUSG00000005672 and 16590, KIT and IDBG-642326 and ENSBTAG00000002699 and 280832
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase
  • Synonyms gene name
    • mannosyl (beta-1,4-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1993-08-27
  • Entrez gene record
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • Mannosyl-glycoprotein N-acetylglucosaminyltransferases
  • VEGA ID
Gene info
Gene info
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    caspase 5
  • Synonyms gene name
    • caspase 5, apoptosis-related cysteine protease
    • caspase 5, apoptosis-related cysteine peptidase
  • Synonyms
  • Locus
  • Discovery year
    1996-09-13
  • Entrez gene record
    838
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • Caspases
    • Caspase recruitment domain containing
  • VEGA ID
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    immunoglobulin heavy variable (III)-82 (pseudogene)
  • Synonyms gene name
    • immunoglobulin heavy variable (III)-82
    • immunoglobulin heavy variable (III)-82 pseudogene
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    2000-04-17
  • Entrez gene record
  • RefSeq identity
  • Classification
    • Immunoglobulin heavy locus at 14q32.33
  • VEGA ID
Gene info
  • Identity
  • Gene
  • Long gene name
    mitochondrially encoded conserved sequence block III
  • Synonyms gene
  • Synonyms gene name
    • conserved sequence block III
  • Synonyms
  • Locus
  • Discovery year
    1989-10-11
  • Pubmed identfication
  • Classification
    • Mitochondrially encoded regions
Gene info
  • Identity
  • Gene
  • Long gene name
    immunoglobulin heavy variable (III)-67-4 (pseudogene)
  • Synonyms gene name
    • immunoglobulin heavy variable (III)-67-4
    • immunoglobulin heavy variable (III)-67-4 pseudogene
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    2000-04-17
  • Entrez gene record
  • RefSeq identity
  • Classification
    • Immunoglobulin heavy locus at 14q32.33
  • VEGA ID
MeSH Data
  • Name
  • 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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