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TIB MOLBIOL fluorescent probes
Fluorescent Probes, supplied by TIB MOLBIOL, 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/fluorogenic+probe/fluorogenic+probes/pm21848694-90-13-32
Average 90 stars, based on 1 article reviews
fluorescent probes - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Polymerase Chain Reaction:

Article Title: Methylprednisolone induces apoptosis by interacting with the JAK/STAT pathway in HL-60 and K-562 leukemic cells.
Article Snippet: Objective: To determine the gene expression profiles of the JAK/STAT pathway members STAT3, STAT5A, STAT5B at both mRNA and protein levels in HL-60 and K-562 leukemia cells that were undergoing apoptosis following high-dose methylprednisolone (MP) treatment.. Methods: HL-60 cells were treated with 0.1 mM MP and K-562 cells were treated with 0.4 mM MP according to their IC50 values.. STAT3, STAT5A, and STAT5B mRNA relative expression levels were determined by qRTPCR whereas the protein levels were detected via western-blot analysis and apoptosis was evaluated by Annexin V method.

Hybridization:

Article Title: Methylprednisolone induces apoptosis by interacting with the JAK/STAT pathway in HL-60 and K-562 leukemic cells.
Article Snippet: Objective: To determine the gene expression profiles of the JAK/STAT pathway members STAT3, STAT5A, STAT5B at both mRNA and protein levels in HL-60 and K-562 leukemia cells that were undergoing apoptosis following high-dose methylprednisolone (MP) treatment.. Methods: HL-60 cells were treated with 0.1 mM MP and K-562 cells were treated with 0.4 mM MP according to their IC50 values.. STAT3, STAT5A, and STAT5B mRNA relative expression levels were determined by qRTPCR whereas the protein levels were detected via western-blot analysis and apoptosis was evaluated by Annexin V method.

Article Title: OPRM1 c.118A>G Polymorphism and Duration of Morphine Treatment Associated with Morphine Doses and Quality-of-Life in Palliative Cancer Pain Settings
Article Snippet: .. The reaction mixture (10 μL) contained Fast Start Taq polymerase (10×), buffer and dNTPs, MgCl 2 (10 mM); Lightcycler Fast Start DNA Master Hybridization Probes Kit ® (catalogue no. 03 003 248 001, Roche Diagnostics GmbH), and 0.2 μL of each primer (20 mM) and fluorescent probes (anchor and sensor, 20 mM) (TIB Molbiol ® , TIBMOLBIOL, Berlin, Germany). .. The samples were then loaded into composite plastic/glass capillaries (20 μL LC capillaries, Roche Diagnosis, catalogue no. 04 929 292 001, Roche Diagnostics GmbH), centrifuged, and were placed in the LightCycler sample carousel.

Article Title: Frequency of CYP2C9 and VKORC1 gene polymorphisms and their influence on warfarin dose in Egyptian pediatric patients.
Article Snippet: Introduction Warfarin is a widely used anticoagulant that shows a high inter-individual variability in the dose needed to achieve target anticoagulation.. In adults, common genetic variants in the cytochrome P450-2C9 (CYP2C9) and vitamin K epoxide reductase complex (VKORC1) enzymes, in addition to non-genetic factors, explain this dose variability.. In children, data about warfarin pharmacogenetics are limited and inconsistent.

Real-time Polymerase Chain Reaction:

Article Title: Nicotinergic Modulation of Attention-Related Neural Activity Differentiates Polymorphisms of DRD2 and CHRNA4 Receptor Genes
Article Snippet: .. The polymorphisms in the CHRNA4 and DRD2 genes were genotyped based on the DNA of buccal cells by means of real time PCR (Light Cycler System, Roche Diagnostics, Mannheim, Germany) using fluorescent probes besides conventional primers (TIB-MOLBIOL, Berlin, Germany). ..

Synthesized:

Article Title: 2-arachidonoylglycerol signaling in forebrain regulates systemic energy metabolism
Article Snippet: .. Primers and fluorogenic probes were synthesized by TIB Molbiol (Adelphia, NJ) or purchased from Applied Biosystems (TaqMan(R) Gene Expression Assays, Foster City, CA) ( Table S5 ). ..

Article Title: Genetic low nephron number hypertension is associated with altered expression of osteopontin and CD44 during nephrogenesis.
Article Snippet: Aims : The study set out to investigate whether the osteopontin (OPN)-CD44-integrin-receptor-system is differently regulated during nephrogenesis in inborn nephron deficit, a major determinant of human primary hypertension and cardiovascular disease in adult life.. Methods : We compared a genetic rat model with an inherited nephron deficit, the Munich-Wistar-Froemter rat (MWF), to normotensive Wistar rats during nephrogenesis at day 19 of fetal development (E19) and at postpartal day 7 (D7).. Results : Renal OPN mRNA ( – 75 % , P < 0.05) and protein expression ( – 38 % , P < 0.05) were strongly decreased at E19 in MWF compared to Wistar.

Article Title: Genetic low nephron number hypertension is associated with altered expression of key components of the renin-angiotensin system during nephrogenesis.
Article Snippet: Aim: This study investigates key components of the reninangiotensin system (RAS) which play a central role in nephrogenesis and possibly in fetal programming of arterial hypertension in adult life.. Methods: We compared a genetic rat model with inborn nephron deficit, the Munich Wistar Fromter rat (MWF), to normotensive Wistar rats during nephrogenesis at day 19 of fetal development (E19) and at postnatal day 7 (D7).. Results: At E19 renal mRNA of angiotensin II type 1a (AT1a) (–50%, P < 0.05) and type 1b (AT1b) (–55%, P < 0.05) receptors were significantly decreased and renal mRNA expression of angiotensin II type 2 (AT2) receptor was fivefold increased in MWF (n = 8) as compared to Wistar rats (n = 8).

Gene Expression:

Article Title: 2-arachidonoylglycerol signaling in forebrain regulates systemic energy metabolism
Article Snippet: .. Primers and fluorogenic probes were synthesized by TIB Molbiol (Adelphia, NJ) or purchased from Applied Biosystems (TaqMan(R) Gene Expression Assays, Foster City, CA) ( Table S5 ). ..

Quantitative RT-PCR:

Article Title: Nipah virus Bangladesh infection elicits organ-specific innate and inflammatory responses in the marmoset model
Article Snippet: RNA was extracted from tissues homogenized in TRIzol reagent or from blood and swabs mixed with TRIzol LS reagent using Direct-zol RNA Miniprep kits (Zymo Research, Irvine, CA). .. RT-qPCR assays were then run using QuantiFast RT-PCR mix (Qiagen, Hilden, Germany), probes targeting NiV M P gene (5′-ACATACAACTGGACCCARTGGTT-3′ and 5′-CACCCTCTCTCAGGGCTTGA-3′) (IDT, Coralville, IA), and fluorescent probe (5′-6FAM-ACAGACGTTGTATA + C + CAT + G-TMR) (TIB MOLBIOL, Adelphia, NJ). .. RT-qPCR was performed using the following cycle: 10 minutes at 50 °C, 5 minutes at 95 °C, and 40 cycles of 10 seconds at 95 °C and 30 seconds at 60 °C using a BioRad CFX96 real time system.

Reverse Transcription Polymerase Chain Reaction:

Article Title: Nipah virus Bangladesh infection elicits organ-specific innate and inflammatory responses in the marmoset model
Article Snippet: RNA was extracted from tissues homogenized in TRIzol reagent or from blood and swabs mixed with TRIzol LS reagent using Direct-zol RNA Miniprep kits (Zymo Research, Irvine, CA). .. RT-qPCR assays were then run using QuantiFast RT-PCR mix (Qiagen, Hilden, Germany), probes targeting NiV M P gene (5′-ACATACAACTGGACCCARTGGTT-3′ and 5′-CACCCTCTCTCAGGGCTTGA-3′) (IDT, Coralville, IA), and fluorescent probe (5′-6FAM-ACAGACGTTGTATA + C + CAT + G-TMR) (TIB MOLBIOL, Adelphia, NJ). .. RT-qPCR was performed using the following cycle: 10 minutes at 50 °C, 5 minutes at 95 °C, and 40 cycles of 10 seconds at 95 °C and 30 seconds at 60 °C using a BioRad CFX96 real time system.



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Image Search Results


(A) Schematic representation of staining procedure for virus-containing supernatant. Supernatant from infected cells is harvested and centrifugated to remove cellular debris. Staining reagents are added to the sample, fixed with paraformaldehyde (PFA) and diluted in DPBS before being analyzed by flow virometry (FVM). (B) Graphical summary of different labelling techniques for targeting the SARS-CoV-2 spike protein via antibodies, the viral RNA genome via the nucleic acid intercalating dye Syto24 and the viral lipid envelope via the lipid intercalating dye MemGlow-488. (C) Dot plots and MFI of D614G stained with monoclonal antibody Tixagevimab (1 µg/mL; anti-RBD) conjugated to DyLight488 (DL488), with Syto24 (20 µM), with MemGlow-488 (200 nM), respectively.

Journal: medRxiv

Article Title: Detection and characterization of single SARS-CoV-2 viral particles by flow virometry

doi: 10.64898/2026.04.28.26351941

Figure Lengend Snippet: (A) Schematic representation of staining procedure for virus-containing supernatant. Supernatant from infected cells is harvested and centrifugated to remove cellular debris. Staining reagents are added to the sample, fixed with paraformaldehyde (PFA) and diluted in DPBS before being analyzed by flow virometry (FVM). (B) Graphical summary of different labelling techniques for targeting the SARS-CoV-2 spike protein via antibodies, the viral RNA genome via the nucleic acid intercalating dye Syto24 and the viral lipid envelope via the lipid intercalating dye MemGlow-488. (C) Dot plots and MFI of D614G stained with monoclonal antibody Tixagevimab (1 µg/mL; anti-RBD) conjugated to DyLight488 (DL488), with Syto24 (20 µM), with MemGlow-488 (200 nM), respectively.

Article Snippet: For staining of SARS-CoV-2 particles, cell culture supernatants were incubated with Tixagevimab conjugated to DyLight-488 (1 μg/mL) or Syto24 (20 μM; Thermo Fisher S7559) or MemGlow-488 (200 nM; Cytoskeleton #MG01) for 30 minutes at room temperature (RT).

Techniques: Staining, Virus, Infection