ncode mirna labeling system Search Results


ncode mirna first-strand cdna synthesis qrt-pcr kit  (Thermo Fisher)
98
Thermo Fisher ncode mirna first-strand cdna synthesis qrt-pcr kit
(A) <t>qRT-PCR</t> analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.
Ncode Mirna First Strand Cdna Synthesis Qrt Pcr Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ncode+mirna+labeling+system/pmc03789769-170-17-19?v=Thermo+Fisher
Average 98 stars, based on 1 article reviews
ncode mirna first-strand cdna synthesis qrt-pcr kit - by Bioz Stars, 2026-07
98/100 stars
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ncode mirna microarray controls  (Genisphere llc)
90
Genisphere llc ncode mirna microarray controls
(A) <t>qRT-PCR</t> analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.
Ncode Mirna Microarray Controls, supplied by Genisphere llc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ncode+mirna+labeling+system/pmc02946509-67-8-24?v=Genisphere+llc
Average 90 stars, based on 1 article reviews
ncode mirna microarray controls - by Bioz Stars, 2026-07
90/100 stars
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ncode vilo mirna complementary dna synthesis kit  (Thermo Fisher)
99
Thermo Fisher ncode vilo mirna complementary dna synthesis kit
(A) <t>qRT-PCR</t> analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.
Ncode Vilo Mirna Complementary Dna Synthesis Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ncode+mirna+labeling+system/10__1016_slash_j__bgm__2013__07__006-30-9-16?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
ncode vilo mirna complementary dna synthesis kit - by Bioz Stars, 2026-07
99/100 stars
  Buy from Supplier
ncode™ sybr® green mirna q pcr kit  (Thermo Fisher)
99
Thermo Fisher ncode™ sybr® green mirna q pcr kit
(A) <t>qRT-PCR</t> analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.
Ncode™ Sybr® Green Mirna Q Pcr Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ncode+mirna+labeling+system/pm28683566-288-8-14?v=Thermo+Fisher
Average 99 stars, based on 1 article reviews
ncode™ sybr® green mirna q pcr kit - by Bioz Stars, 2026-07
99/100 stars
  Buy from Supplier
ncode™ sybr ® green mirna quantitative real-time pcr (qrtpcr) kit  (Thermo Fisher)
97
Thermo Fisher ncode™ sybr ® green mirna quantitative real-time pcr (qrtpcr) kit
(A) <t>qRT-PCR</t> analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.
Ncode™ Sybr ® Green Mirna Quantitative Real Time Pcr (Qrtpcr) Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ncode+mirna+labeling+system/pm25234714-46-8-10?v=Thermo+Fisher
Average 97 stars, based on 1 article reviews
ncode™ sybr ® green mirna quantitative real-time pcr (qrtpcr) kit - by Bioz Stars, 2026-07
97/100 stars
  Buy from Supplier
ncode mirna qrt-pcr analysis  (Ribobio co)
90
Ribobio co ncode mirna qrt-pcr analysis
(A) <t>qRT-PCR</t> analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.
Ncode Mirna Qrt Pcr Analysis, supplied by Ribobio co, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ncode+mirna+labeling+system/pm30362152-28-10-15?v=Ribobio+co
Average 90 stars, based on 1 article reviews
ncode mirna qrt-pcr analysis - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


(A) qRT-PCR analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.

Journal: PLoS Pathogens

Article Title: Bacterial Pathogens Activate a Common Inflammatory Pathway through IFNλ Regulation of PDCD4

doi: 10.1371/journal.ppat.1003682

Figure Lengend Snippet: (A) qRT-PCR analysis of IFNλ mRNA in BMDCs stimulated with heat killed USA300, µ ± SD. (B) ELISA analysis of IFNλ in BAL of WT mice following 4 and 18 hours of infection with USA300. (C) Numbers (CFU) of USA300 recovered from BAL of WT and IL-28R −/− mice following 4 and 18 hours of infection. (D) Numbers (CFU) of USA300 recovered from lung tissue of WT and IL-28R −/− mice following 4 and 18 hours of infection. (E) Trichrome stained lungs from WT and IL-28R −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (F) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in BAL of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. (G) Numbers of dendritic cells (DC), macrophages (MAC), and neutrophils in lung tissue of WT and IL-28R −/− in unstimulated (NS) mice or following 4 or 18 hours of infection. Data are representative of at least 2 independent experiments.

Article Snippet: For miRNA analysis cDNA was generated and qRT-PCR was run using NCode miRNA First-Strand cDNA Synthesis and qRT-PCR Kit (Life Technologies) according to the manufacturers instructions.

Techniques: Quantitative RT-PCR, Enzyme-linked Immunosorbent Assay, Infection, Staining

(A) qRT-PCR analysis of IL-8 in 16HBE cells treated with control or PDCD4 siRNA and infected with USA300, µ ± SD. (B) qRT-PCR analysis of miR-21 in 16HBE cells treated with recombinant IFNλ for 1 hour, µ ± SD. (C) Western blot analysis of PDCD4 in 16HBE cells treated with recombinant IFNλ. (D) qRT-PCR analysis of miR-21 in 16HBE cells pretreated with STAT3 inhibitor or DMSO treated with recombinant IFNλ for 1 hour, µ ± SD. (E) Western blot analysis of PDCD4 in 16HBE cells pretreated with STAT3 inhibitor or DMSO treated with recombinant IFNλ for 1 hour. Lysate from 16HBE cells treated with DMSO and IFNλ was used as a positive control (pos). (F) Western blot analysis of PDCD4 in human epithelial cells (16HBE) following stimulation with S. aureus protein A (SpA), µ ± SD. (G) Western blot analysis of PDCD4 in 16HBE cells treated with anti-TNFR1 or control IgG and SPA for 2 hours, µ ± SD. Data are representative of at least 2 independent experiments.

Journal: PLoS Pathogens

Article Title: Bacterial Pathogens Activate a Common Inflammatory Pathway through IFNλ Regulation of PDCD4

doi: 10.1371/journal.ppat.1003682

Figure Lengend Snippet: (A) qRT-PCR analysis of IL-8 in 16HBE cells treated with control or PDCD4 siRNA and infected with USA300, µ ± SD. (B) qRT-PCR analysis of miR-21 in 16HBE cells treated with recombinant IFNλ for 1 hour, µ ± SD. (C) Western blot analysis of PDCD4 in 16HBE cells treated with recombinant IFNλ. (D) qRT-PCR analysis of miR-21 in 16HBE cells pretreated with STAT3 inhibitor or DMSO treated with recombinant IFNλ for 1 hour, µ ± SD. (E) Western blot analysis of PDCD4 in 16HBE cells pretreated with STAT3 inhibitor or DMSO treated with recombinant IFNλ for 1 hour. Lysate from 16HBE cells treated with DMSO and IFNλ was used as a positive control (pos). (F) Western blot analysis of PDCD4 in human epithelial cells (16HBE) following stimulation with S. aureus protein A (SpA), µ ± SD. (G) Western blot analysis of PDCD4 in 16HBE cells treated with anti-TNFR1 or control IgG and SPA for 2 hours, µ ± SD. Data are representative of at least 2 independent experiments.

Article Snippet: For miRNA analysis cDNA was generated and qRT-PCR was run using NCode miRNA First-Strand cDNA Synthesis and qRT-PCR Kit (Life Technologies) according to the manufacturers instructions.

Techniques: Quantitative RT-PCR, Infection, Recombinant, Western Blot, Positive Control

(B) qRT-PCR analysis of PDCD4 mRNA in the lungs of WT and IL-28R −/− mice following infection with USA300, µ ± SD. (C) Western blot analysis of PDCD4 in the lungs of WT and IL-28R −/− mice following infection with USA300, µ ± SD. (D) Numbers (CFU) of USA300 recovered from BAL of WT and PDCD4 −/− mice following 18 hours of infection. (E) Numbers (CFU) of USA300 recovered from lung tissue of WT and PDCD4 −/− mice following 18 hours of infection. (F) Trichrome stained lungs from WT and PDCD4 −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (G) ELISA analysis of individual cytokines in BAL of WT and PDCD4 −/− mice. Data are representative of at least 2 independent experiments.

Journal: PLoS Pathogens

Article Title: Bacterial Pathogens Activate a Common Inflammatory Pathway through IFNλ Regulation of PDCD4

doi: 10.1371/journal.ppat.1003682

Figure Lengend Snippet: (B) qRT-PCR analysis of PDCD4 mRNA in the lungs of WT and IL-28R −/− mice following infection with USA300, µ ± SD. (C) Western blot analysis of PDCD4 in the lungs of WT and IL-28R −/− mice following infection with USA300, µ ± SD. (D) Numbers (CFU) of USA300 recovered from BAL of WT and PDCD4 −/− mice following 18 hours of infection. (E) Numbers (CFU) of USA300 recovered from lung tissue of WT and PDCD4 −/− mice following 18 hours of infection. (F) Trichrome stained lungs from WT and PDCD4 −/− mice following and 18 hour USA300 infection (original magnification 100x, insert 400x). (G) ELISA analysis of individual cytokines in BAL of WT and PDCD4 −/− mice. Data are representative of at least 2 independent experiments.

Article Snippet: For miRNA analysis cDNA was generated and qRT-PCR was run using NCode miRNA First-Strand cDNA Synthesis and qRT-PCR Kit (Life Technologies) according to the manufacturers instructions.

Techniques: Quantitative RT-PCR, Infection, Western Blot, Staining, Enzyme-linked Immunosorbent Assay

(A) ELISA analysis of individual cytokines in BAL of WT and IL-28R −/− mice. (B) Western blot analysis of MX1 expression in lungs of WT and IL-28R −/− mice following 4 and 18 hours of infection with PAK. (C) qRT-PCR analysis of IL-8 in 16HBE cells treated with control or PDCD4 siRNA and infected with PAK, µ ± SD. (D) qRT-PCR analysis of miR-21 in the lungs of WT and IL-28R −/− mice following infection with PAK, µ ± SD. (E) qRT-PCR analysis of PDCD4 mRNA in the lungs of WT and IL-28R −/− mice following infection with PAK, µ ± SD. (F) Western blot analysis of PDCD4 in the lungs of WT and IL-28R −/− mice following infection with PAK, µ ± SD. (G) Western blot analysis of phosphorylation of p70S6K in 16HBE cells treated with recombinant IFNλ. (H) Western blot analysis of phosphorylation of p70S6K and PDCD4 in the lungs of WT and IL-28R −/− mice following infection with PAK. (I) Western blot analysis of phosphorylation of p70S6K and PDCD4 in the lungs of WT and IL-28R −/− mice following infection with USA300. Data are representative of at least 2 independent experiments.

Journal: PLoS Pathogens

Article Title: Bacterial Pathogens Activate a Common Inflammatory Pathway through IFNλ Regulation of PDCD4

doi: 10.1371/journal.ppat.1003682

Figure Lengend Snippet: (A) ELISA analysis of individual cytokines in BAL of WT and IL-28R −/− mice. (B) Western blot analysis of MX1 expression in lungs of WT and IL-28R −/− mice following 4 and 18 hours of infection with PAK. (C) qRT-PCR analysis of IL-8 in 16HBE cells treated with control or PDCD4 siRNA and infected with PAK, µ ± SD. (D) qRT-PCR analysis of miR-21 in the lungs of WT and IL-28R −/− mice following infection with PAK, µ ± SD. (E) qRT-PCR analysis of PDCD4 mRNA in the lungs of WT and IL-28R −/− mice following infection with PAK, µ ± SD. (F) Western blot analysis of PDCD4 in the lungs of WT and IL-28R −/− mice following infection with PAK, µ ± SD. (G) Western blot analysis of phosphorylation of p70S6K in 16HBE cells treated with recombinant IFNλ. (H) Western blot analysis of phosphorylation of p70S6K and PDCD4 in the lungs of WT and IL-28R −/− mice following infection with PAK. (I) Western blot analysis of phosphorylation of p70S6K and PDCD4 in the lungs of WT and IL-28R −/− mice following infection with USA300. Data are representative of at least 2 independent experiments.

Article Snippet: For miRNA analysis cDNA was generated and qRT-PCR was run using NCode miRNA First-Strand cDNA Synthesis and qRT-PCR Kit (Life Technologies) according to the manufacturers instructions.

Techniques: Enzyme-linked Immunosorbent Assay, Western Blot, Expressing, Infection, Quantitative RT-PCR, Recombinant