igScript™ One Step RT-qPCR Kit - 100 Reactions

• Catalog number
  4214
• Price
  Please ask
• Size
  100 reactions

• Description
  igScript™ one step RT-qPCR kit combines two powerful mixtures: i). igScript™ Reverse Transcriptase and ii) ig SYBR® Green qPCR 2x master mix with standard buffer providing improved PCR efficiency, wider dynamic range, superior sensitivity and specificity. The two mixtures require minimal handling during reaction setup and offer consistent and robust RT-qPCR reactions. Product Includes: ig Script™ Reverse Transcriptase ig SYBR™ Green qPCR 2x Master Mix
• Shipping Condition
  Ships with Dry Ice

• Gene target
  igScript™   One   RT-qPCR   Kit   100  
• Gene symbol
  SNRPN
• Short name
  igScript™ One Step RT-qPCR Kit - 100
• Technique
  step, steps
• Alternative name
  igScript™ One Step Reverse transcription quantitative PCR test kit reagent - 100 Reactions
• Alternative technique
  steps, kits
• 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

• Identity
  HGNC:11164
• Gene
  SNRPN
• Long gene name
  small nuclear ribonucleoprotein polypeptide N
• Synonyms gene
  • PWCR
• Synonyms gene name
  • Prader-Willi syndrome chromosome region
• Synonyms
  • SMN
  • SM-D
  • HCERN3
  • SNRNP-N
  • SNURF-SNRPN
  • RT-LI
• Synonyms name
  • tissue-specific splicing protein
  • SM protein N
  • small nuclear ribonucleoprotein N
• GenBank acession
  • L80005
• Locus
  15q11.2
• Discovery year
  1992-08-24
• Entrez gene record
  6638
• Pubmed identfication
  • 1533223
• RefSeq identity
  • NM_003097
• Classification
  • Sm spliceosomal proteins
• VEGA ID
  OTTHUMG00000129180

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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