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diffquik staining kit  (Imeb Inc)

 
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    Imeb Inc diffquik staining kit
    Diffquik Staining Kit, supplied by Imeb Inc, 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/diffquik+staining+kit/diffquick+staining+kit/pm40349650-119-27-30
    Average 90 stars, based on 1 article reviews
    diffquik staining kit - by Bioz Stars, 2026-09
    90/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Quantifying mechanical, proliferation, and migrational properties of bulk ovarian cancer cells and ovarian cancer stem cells.
    Article Snippet: There are a limited number of studies analyzing ovarian cancer stem cell properties.. The goal of this study was to analyze the mechanical and migrational properties of ovarian cancer stem cells with the well-researched bulk ovarian cancer cells.. Through the use of atomic force microscopy (AFM), the mechanical properties of both cell types were gathered.

    Article Title: Proteomic analysis of human macrophages exposed to hypochlorite-oxidized low-density lipoprotein.
    Article Snippet: Article history: The invasion of monocytes t Received 15 July 2008 Received in revised form 14 October 2008 Accepted 14 November 2008 Available online 6 December 2008

    Article Title: Characterization of Quin-C1 for its anti-inflammatory property in a mouse model of bleomycin-induced lung injury.
    Article Snippet: To facilitate cell counting, the remaining red blood cells were eliminated with lysis buffer (Beyotime Institute of Biotechnology, Haimen, China). .. Total and differential cell counts (neutrophils, lymphocytes and macrophages) in the BALF were determined with the DiffQuick Stain Kit (IMEB Inc, San Marcos, CA, USA). ..

    Article Title: Epidermal Growth Factor-Like Domain Repeat of Stabilin-2 Recognizes Phosphatidylserine during Cell Corpse Clearance
    Article Snippet: .. The cells were then fixed with methanol and stained by using a DiffQuick staining kit (IMEB, Inc.). ..

    Article Title: Cross Talk between Engulfment Receptors Stabilin-2 and Integrin ?v?5 Orchestrates Engulfment of Phosphatidylserine-Exposed Erythrocytes
    Article Snippet: .. The cells were then fixed with methanol and stained by using a DiffQuick staining kit (IMEB, Inc.). ..

    Article Title: Inhibition of chemotherapy resistant breast cancer stem cells by a ROR1 specific antibody
    Article Snippet: .. Invasive cells were fixed with 4% paraformaldehyde and stained by DiffQuick staining kits (IMEB Inc, San Marcos, CA) and visualized with an inverted microscope (Nikon). ..

    Article Title: Cross Talk between Engulfment Receptors Stabilin-2 and Integrin αvβ5 Orchestrates Engulfment of Phosphatidylserine-Exposed Erythrocytes
    Article Snippet: .. The cells were then fixed with methanol and stained by using a DiffQuick staining kit (IMEB, Inc.). ..

    Transformation Assay:

    Article Title: Proteomic analysis of human macrophages exposed to hypochlorite-oxidized low-density lipoprotein.
    Article Snippet: Article history: The invasion of monocytes t Received 15 July 2008 Received in revised form 14 October 2008 Accepted 14 November 2008 Available online 6 December 2008

    Incubation:

    Article Title: Proteomic analysis of human macrophages exposed to hypochlorite-oxidized low-density lipoprotein.
    Article Snippet: Article history: The invasion of monocytes t Received 15 July 2008 Received in revised form 14 October 2008 Accepted 14 November 2008 Available online 6 December 2008

    Inverted Microscopy:

    Article Title: Inhibition of chemotherapy resistant breast cancer stem cells by a ROR1 specific antibody
    Article Snippet: .. Invasive cells were fixed with 4% paraformaldehyde and stained by DiffQuick staining kits (IMEB Inc, San Marcos, CA) and visualized with an inverted microscope (Nikon). ..



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    Effects of forced expression of ALDH1A2 on invasive potential of ovarian cancer cells. ( A , B ) Invasion assay; RMG-I cells transfected with either the empty vector or ALDH1A2 expression vector for 24 h were loaded into the upper chamber and then fetal bovine serum (FBS, 5%) was added to the lower chamber. After 24 h, the cells that invaded the lower chamber were stained with <t>DiffQuik</t> ( A ) and quantified ( B ) under a microscope. Data are expressed as means ± SD. Statistical significance was assessed using an unpaired t -test. *** p < 0.005. ( C ) Sprouting assay; RMG1 cells ectopically expressing ALDH1A2 were embedded with Matrigel and incubated for 24 h. Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm. ( D ) Sprouting assay using RMG1 cells incubated in the presence or absence of ATRA (1 μM, 5 μM). Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm.
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    Effects of forced expression of ALDH1A2 on invasive potential of ovarian cancer cells. ( A , B ) Invasion assay; RMG-I cells transfected with either the empty vector or ALDH1A2 expression vector for 24 h were loaded into the upper chamber and then fetal bovine serum (FBS, 5%) was added to the lower chamber. After 24 h, the cells that invaded the lower chamber were stained with <t>DiffQuik</t> ( A ) and quantified ( B ) under a microscope. Data are expressed as means ± SD. Statistical significance was assessed using an unpaired t -test. *** p < 0.005. ( C ) Sprouting assay; RMG1 cells ectopically expressing ALDH1A2 were embedded with Matrigel and incubated for 24 h. Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm. ( D ) Sprouting assay using RMG1 cells incubated in the presence or absence of ATRA (1 μM, 5 μM). Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm.
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    Image Search Results


    Effects of forced expression of ALDH1A2 on invasive potential of ovarian cancer cells. ( A , B ) Invasion assay; RMG-I cells transfected with either the empty vector or ALDH1A2 expression vector for 24 h were loaded into the upper chamber and then fetal bovine serum (FBS, 5%) was added to the lower chamber. After 24 h, the cells that invaded the lower chamber were stained with DiffQuik ( A ) and quantified ( B ) under a microscope. Data are expressed as means ± SD. Statistical significance was assessed using an unpaired t -test. *** p < 0.005. ( C ) Sprouting assay; RMG1 cells ectopically expressing ALDH1A2 were embedded with Matrigel and incubated for 24 h. Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm. ( D ) Sprouting assay using RMG1 cells incubated in the presence or absence of ATRA (1 μM, 5 μM). Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm.

    Journal: Cancers

    Article Title: ALDH1A2 Is a Candidate Tumor Suppressor Gene in Ovarian Cancer

    doi: 10.3390/cancers11101553

    Figure Lengend Snippet: Effects of forced expression of ALDH1A2 on invasive potential of ovarian cancer cells. ( A , B ) Invasion assay; RMG-I cells transfected with either the empty vector or ALDH1A2 expression vector for 24 h were loaded into the upper chamber and then fetal bovine serum (FBS, 5%) was added to the lower chamber. After 24 h, the cells that invaded the lower chamber were stained with DiffQuik ( A ) and quantified ( B ) under a microscope. Data are expressed as means ± SD. Statistical significance was assessed using an unpaired t -test. *** p < 0.005. ( C ) Sprouting assay; RMG1 cells ectopically expressing ALDH1A2 were embedded with Matrigel and incubated for 24 h. Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm. ( D ) Sprouting assay using RMG1 cells incubated in the presence or absence of ATRA (1 μM, 5 μM). Phase contrast images were observed (left panel). Calcein-AM-stained cells were visualized using a fluorescence microscope (right panel). Original magnification: 4×. Scale bar, 500 μm.

    Article Snippet: After 24 h, the membranes were fixed with 100% methanol and stained with a DiffQuik stain kit (Triangle Biomedical Sciences, Inc., Durham, NC, USA).

    Techniques: Expressing, Invasion Assay, Transfection, Plasmid Preparation, Staining, Microscopy, Incubation, Fluorescence