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li cor image studio acquisition software  (LI-COR)


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    Structured Review

    LI-COR li cor image studio acquisition software
    Li Cor Image Studio Acquisition Software, supplied by LI-COR, used in various techniques. Bioz Stars score: 98/100, based on 550 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/li+cor+acquisition+software/Odyssey+CLx+Image+Studio+Analysis+Software+-+In-Cell+Western+Add-On/pm41995846-101-12-18
    Average 98 stars, based on 550 article reviews
    li cor image studio acquisition software - by Bioz Stars, 2026-09
    98/100 stars

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    Related Articles

    Software:

    Article Title: Hemin-induced platelet activation is regulated via ACKR3 chemokine surface receptor - implications for passivation of vulnerable atherosclerotic plaque
    Article Snippet: Equal loading was verified by actin (Abcam, Cambridge, UK) immunostaining. .. After drying the blots were detected by the Li-COR Odyssey System (LI-COR Biotechnology – GmbH, Bad Homburg, Germany) and analyzed by Li-COR Acquisition software (Version 5.2). .. Statistical analysis and the graphical data design were performed with GraphPad Prism (Graphpad Software, Inc., La Jolla, CA, USA, Version 10.1.1).

    Article Title: Cap-independent co-expression of dsRNA-sensing and NF-κB pathway inhibitors enables controllable self-amplifying RNA expression with reduced immunotoxicity
    Article Snippet: In a separate tube, 3 μL of Lipofectamine MessengerMAX (Invitrogen) was diluted in 100 μL of Opti-MEM I. .. Imaging was performed using an Odyssey M laser scanner (LI-COR), using LI-COR acquisition software, a plate offset of +1.45 mm, and 100 μm resolution. ..

    Article Title: The Unkempt RNA binding protein reveals a local translation program in centriole overduplication
    Article Snippet: .. After 3 TBST washes, blots were incubated in Licor IR680 or IR800 secondary antibodies at 1:20,000 for 1 hour, washed 3 times with TBST and imaged using a fluorescence Odyssey CLx Imager and LI-COR Acquisition Software (LICORbio). .. RNA used for polyA-selected library generation for mRNA sequencing was isolated with the Monarch Total RNA isolation miniprep kit (New England Biolabs).

    Article Title: Automated Transcranial Photobiomodulation in Healthy Rats: Effects on Working Memory and Brain Markers
    Article Snippet: The second day, the membranes were incubated with the appropriate secondary antibodies (Licor 926-68070 mouse IRDye680RD 1:20.000, Licor 926-32211 rabbit IRDye800CW 1:20.000, Licor IRDye800CW 926-32210 mouse 1:20.000, Licor IRDye680RD rabbit 926-68071 1:20.000) for 1 h at room temperature. .. The membranes were then washed (5 min/wash, 2 times in total) and visualized using Image Lab software with LI-COR Acquisition Software (Odyssey Imager). ..

    Article Title: Respiratory viruses activate autophagy via the IFN-STAT1/STAT5B-SOCS1 axis
    Article Snippet: In brief, whole cell lysates were mixed with 6x Protein Sample Loading Buffer (Tris-HCl pH 6.8, 75% Glycerol, 6% SDS, 0,3% w(v) Orange G, 15% β-mercaptoethanol) and heated to 96°C for 10 min, separated on NuPAGE 4-12% Bis-Tris Gels (Invitrogen) for 90-120 minutes at 90 V and transferred onto Immobilon-FL PVDF membranes (Merck Millipore) at a constant voltage of 30 V for 30 min. After the transfer, the membrane was dried overnight at room temperature and total protein staining was performed using the Revert 700 Total Protein Stain (LI-COR) according to the manufacturer’s instructions. .. Detection of proteins was done using either an Odyssey 9120 Imager (LI-COR) with the Image Studio software (Version 5.2, LI-COR) or an Odyssey M Imaging System (LI-COR) with the LI-COR Acquisition software (Version 2.2, LI-COR). .. Proteins were stained with primary antibodies (mouse anti-SQSTM1/p62, abcam, #ab56416, 1:1000, mouse anti-FLAG M2, Sigma-Aldrich, #F1804, 1:3000, rabbit anti-V5, Cell Signaling, #13202, 1:1000, mouse anti-STAT1, Santa Cruz, #sc-464, 1:250, rabbit anti-STAT2, Cell Signaling, #72604, 1:250, rabbit anti-STAT5B, Genetex, #GTX08967, 1:250, rat anti-GAPDH, BioLegend, #607902, 1:3000) diluted in 0.1% Casein in PBS overnight at 4°C.

    Article Title: Cap-independent co-expression of dsRNA-sensing and NF-κB pathway inhibitors enables controllable self-amplifying RNA expression with reduced immunotoxicity
    Article Snippet: After permeabilization, cells were blocked with Intercept TBS Blocking Buffer (LI- COR) for 1 hr at room temperature with gentle agitation. .. The plate was then imaged using the Odyssey M imager with LI- COR Acquisition software using a plate offset of +1.45 and 100 μm resolution. .. Signal quantification was carried out using Empiria Studio software (LI- COR).

    Imaging:

    Article Title: Cap-independent co-expression of dsRNA-sensing and NF-κB pathway inhibitors enables controllable self-amplifying RNA expression with reduced immunotoxicity
    Article Snippet: In a separate tube, 3 μL of Lipofectamine MessengerMAX (Invitrogen) was diluted in 100 μL of Opti-MEM I. .. Imaging was performed using an Odyssey M laser scanner (LI-COR), using LI-COR acquisition software, a plate offset of +1.45 mm, and 100 μm resolution. ..

    Article Title: Respiratory viruses activate autophagy via the IFN-STAT1/STAT5B-SOCS1 axis
    Article Snippet: In brief, whole cell lysates were mixed with 6x Protein Sample Loading Buffer (Tris-HCl pH 6.8, 75% Glycerol, 6% SDS, 0,3% w(v) Orange G, 15% β-mercaptoethanol) and heated to 96°C for 10 min, separated on NuPAGE 4-12% Bis-Tris Gels (Invitrogen) for 90-120 minutes at 90 V and transferred onto Immobilon-FL PVDF membranes (Merck Millipore) at a constant voltage of 30 V for 30 min. After the transfer, the membrane was dried overnight at room temperature and total protein staining was performed using the Revert 700 Total Protein Stain (LI-COR) according to the manufacturer’s instructions. .. Detection of proteins was done using either an Odyssey 9120 Imager (LI-COR) with the Image Studio software (Version 5.2, LI-COR) or an Odyssey M Imaging System (LI-COR) with the LI-COR Acquisition software (Version 2.2, LI-COR). .. Proteins were stained with primary antibodies (mouse anti-SQSTM1/p62, abcam, #ab56416, 1:1000, mouse anti-FLAG M2, Sigma-Aldrich, #F1804, 1:3000, rabbit anti-V5, Cell Signaling, #13202, 1:1000, mouse anti-STAT1, Santa Cruz, #sc-464, 1:250, rabbit anti-STAT2, Cell Signaling, #72604, 1:250, rabbit anti-STAT5B, Genetex, #GTX08967, 1:250, rat anti-GAPDH, BioLegend, #607902, 1:3000) diluted in 0.1% Casein in PBS overnight at 4°C.

    Incubation:

    Article Title: The Unkempt RNA binding protein reveals a local translation program in centriole overduplication
    Article Snippet: .. After 3 TBST washes, blots were incubated in Licor IR680 or IR800 secondary antibodies at 1:20,000 for 1 hour, washed 3 times with TBST and imaged using a fluorescence Odyssey CLx Imager and LI-COR Acquisition Software (LICORbio). .. RNA used for polyA-selected library generation for mRNA sequencing was isolated with the Monarch Total RNA isolation miniprep kit (New England Biolabs).

    Fluorescence:

    Article Title: The Unkempt RNA binding protein reveals a local translation program in centriole overduplication
    Article Snippet: .. After 3 TBST washes, blots were incubated in Licor IR680 or IR800 secondary antibodies at 1:20,000 for 1 hour, washed 3 times with TBST and imaged using a fluorescence Odyssey CLx Imager and LI-COR Acquisition Software (LICORbio). .. RNA used for polyA-selected library generation for mRNA sequencing was isolated with the Monarch Total RNA isolation miniprep kit (New England Biolabs).

    other:

    Article Title: Cap-independent co-expression of dsRNA-sensing and NF-κB pathway inhibitors enables controllable self-amplifying RNA expression with reduced immunotoxicity
    Article Snippet: For transfection in six- well plates, the medium was removed and replaced with 1 mL of Opti- MEM I (Gibco).

    Article Title: Cap-independent co-expression of dsRNA-sensing and NF-κB pathway inhibitors enables controllable self-amplifying RNA expression with reduced immunotoxicity
    Article Snippet: The following primary antibodies were used: Phospho-eIF2α (Ser51) (D9G8) XP rabbit monoclonal (1:200, #3398, Cell Signaling Technology), eIF2α (L57A5) mouse monoclonal (1:200, #2103, Cell Signaling Technology), PKR rabbit polyclonal (1:500, #18244-1-AP, Proteintech), Phospho-eIF4E (S209) rabbit monoclonal (1:200, #ab76256, Abcam), eIF4E mouse monoclonal (5D11) (1:200, #MA1-089, Invitrogen), and FAP (73.3) mouse monoclonal (20 μg/mL, #BE0374, InVivoMAb).



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