Human Apoptosis3 qPCR array

  • Catalog number
    ANGNH-AP3H1
  • Price
    Please ask
  • Size
    1 x 96 well primer plate
  • Genes
    CFL1, EIF2AK2, FOXO1, GSTP1, HDAC1, HDAC2, HDAC3, HSPA1B, IGF1, IKBKB, IKBKG, IL10, IL2, MAPK14, MAP2K3, MAP3K7, TAB1, AKT1S1, ALOX12, ATF5, BDNF, BECN1, CBX4, CCL2, IL3, IL3RA, PPARA, PTK2, PTK2B, TERT, CARD11, CARD17, CARD18, NOD2, RFWD2, ACTA1, CSF2, CUL1, CUL2, CUL3, ADORA1, AIFM1, APOE, BCL3, BIRC7, BTK, CAPN2, CD14, CD2, CD38, CD5, CEBPG, DAP, DDIT3, EP300, FOXO3, IL1A, MADD, MYD88, PTEN, CEBPB, FOS, GSK3B, HGF, IL2RB, IRAK1, KIT, KITLG, SPP1, SRC, LTB, TNFSF14, TNFSF15, NGFR, TNFRSF18, TNFRSF19, TNFRSF8, ECSIT, ELK1, LY96, TIRAP, TLR2, TOLLIP, TRA
  • Sequence disclosure
    We do not standard disclose the sequence of our carefully selected and oprimized RT PCR primers.
  • Excel template
    We will supply you with a microsoft excel template to analyse the qPCR results and see the activation, or supression of genes of interestof your profiler.
  • Sign Arrays
    signal transduction
  • Custom 96 or 384 well qPCR primers
    1 euro or USD per human gene added to the qPCR Apoptosis3 profiling plate.
  • Roche LightCycler compatibility
    The LightCycler 480, for 96 well qPCR: XXXH1-RXS for 384 well: XXXH2-RXS. With perfect Master Mix Sybr Green: PMSX-WXS, 82 Euro
  • AB cycler RT PCR blocks
    The Applied Biosystems Step One Plus Real-Time System 96 well is used with the qPCR XXXH1-FXS with Perfect Master Mix SYBR Green PMSX-RXS, 82 USD and ABI 7900 HT (standard block) XXXH1-AXS, XXXH2-AXS, PMSX-RXS and ViiA7 system (standard block), XXXH1-AXS, XXXH2-AXS, PMSX-LRXS and QuantStudio 6, 7, 12K Flex System (standard block)
  • Biorad qPCR cyclers
    The RT PCR CFX 96 cycler, CFX 384, CFX Connect, Opticon, Chomo, iQ and MyiQ Cycler are compatible withour Perfect Master Mix SYBR Green. Contact us for the reference.
  • Pathway profiling
    The expression RT PCR profiler array is supplied in 96 and 384 well primer plates. They are used to profile cDNA from human tissues, cells or body fluids. We can perform signaling pathways analysis with only 10-100 cells with the 2018 Direct lysis to SignArray reagent. For rare or precious sampleswe use the SpeAmpn reagents to analyze until 4 signaling pathways with only 5-50ng starting amount of RNA. The adapted hot start SYBR Green qPCR kit apropriate to your Real Time PCR cycler is supplied at 82$ or Euro. Please supply us with your qPCR cyler model when ordering.
  • Pathway profiling outsourcing
    We have a large collection of cell lines and can perfome the Apoptosis3 expression profiling for you. You can send us your tissues or we have a library of tissues and can perform the RNA extraction, make the cDNA and perform the RT-PCR and qPCR for you.
  • QPCR Master Mix
    We suppy PMS reagent or Perfect Master Mix SYBRG for SignArrays 96 at 10 μl of PMS per reaction for 20 μl final volume. The reference is: PMS1-Z2S, 82 euro
  • Single gene qPCR
    Perfect Master Mix PROBE, PMP1-Z50 for 50 reactions, price: 75 eur/USD
  • Distribution
    Gentaur ensures worldwide distribution of Human Apoptosis3 qPCR array except for spain
  • Description
    More than 1 can be supplied by AnyGenes.
  • Properties
    Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.
  • Gene target
  • Short name
    Apoptosis3 qPCR array
  • Technique
    array, arrays
  • Species
    Human, Humans
  • Alternative name
    H. sapiens Apoptosis3 Quantitative real-time PCR test kit array
  • Alternative technique
    arrays
  • Tissue
    array
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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