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Baxter Dade Diagnostic diff-quick kit
Diff Quick Kit, supplied by Baxter Dade Diagnostic, 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/quick-diff/diff+quick+stain+set/pmc08364116-94-6-8
Average 90 stars, based on 1 article reviews
diff-quick kit - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

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Article Title: The apoptotic pathway in fertile and subfertile men: a case-control and prospective study to examine the impact of merocyanine 540 bodies on ejaculated spermatozoa.
Article Snippet: Nardhy Gomez-Lopez, Ph.D., Guadalupe Estrada-Gutierrez, Ph.D., Alinne Colin, M.D., M.Sc., Arturo Flores-Pliego, M.Sc., Xochitl Flores-Escobar, B.Sc., Sergio Oehninger, M.D., Ph.D., and Gerardo Barroso, M.D., M.Sc. a Instituto Nacional de Perinatologia Isidro Espinosa de los Reyes, and b Reproductive Health Division, American British Cowdray Medical Center, Mexico City, Mexico; c Obstetrics and Gynecology, School of Medicine, Wayne State University, Perinatology Research Branch/NICHD/NIH, Detroit, Michigan; and d The Jones Institute of Reproductive Medicine, Eastern Virginia Medical School, Norfolk, Virginia

Article Title: Exendin-4 Induces Cell Adhesion and Differentiation and Counteracts the Invasive Potential of Human Neuroblastoma Cells
Article Snippet: At the end of the 22 h incubation, the non-migrated cells were removed, the migrated cells were fixed with cold methanol and stained using a Diff-Quick kit (Dade Diagnostics of Puerto Rico Inc) and then photographed at 200X magnification using a phase-contrast microscope AxioVision Zeiss (Zeiss Gottingen, Germany).

Article Title: Semen Cryopreservation to Expand Male Fertility in Cancer Patients: Intracase Evaluation of Semen Quality.
Article Snippet: Glass slides were stained using smears in the Diff-Quick Kit (Baxter Dade diagnostics AG, Dubingen, Switzerland).

Article Title: Heparan sulfate side chains have a critical role in the inhibitory effects of perlecan on vascular smooth muscle cell response to arterial injury.
Article Snippet: Lara Gotha,* Sang Yup Lim,* Azriel B. Osherov, Rafael Wolff, Beiping Qiang, Ilana Erlich, Nafiseh Nili, Sivaram Pillarisetti, Ya-Ting Chang, Phan-Kiet Tran, Karl Tryggvason, Ulf Hedin, Karin Tran-Lundmark, Suzanne L. Advani, Richard E. Gilbert, and Bradley H. Strauss Schulich Heart Program, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada; Keenan Research Centre in the Li Ka Shing Knowledge Institute, St. Michael’s Hospital, University of Toronto, Toronto, Ontario, Canada; Dr. Reddy’s Laboratories, Norcross, Georgia; Department of Pediatric Cardiac Surgery, Skane University Hospital, Lund, Sweden; Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden; and Korea University Ansan Hospital, Ansan, Korea

Article Title: Effect of bacterial infection on sperm quality and DNA fragmentation in subfertile men with Leukocytospermia
Article Snippet: The smears were stained by a Diff-quick kit (Baxter Dade diagnostics AG, Dubingen, Switzerland).

Article Title: Phenolic compounds as antiangiogenic CMG2 inhibitors from Costa Rican endophytic fungi.
Article Snippet: Membranes were then fixed and processed using Diff-Quick staining solution (Dade Diagnostics).

Article Title: Semen Cryopreservation to Expand Male Fertility in Cancer Patients: Intracase Evaluation of Semen Quality
Article Snippet: Glass slides were stained using smears in the Diff-Quick Kit (Baxter Dade diagnostics AG, Dubingen, Switzerland).

Staining:

Article Title: Human intestinal myofibroblasts deposited collagen VI enhances adhesiveness for T cells – A novel mechanism for maintenance of intestinal inflammation
Article Snippet: In specific experiments, 5 ng/ml phorbol 12-myristate 13-acetate (PMA, Sigma, St. Louis, MO, USA) was added for 1 h. After 3 h at 37 °C, non-adherent T cells were removed by gentle aspiration and wells rinsed 3 times with Ca ++ - and Mg ++ -containing HBSS. .. T cells were either pre-labeled by calcein (Thermo Fisher Scientific, Waltham, MA, USA) or were stained after adhesion and fixation (Diff Quick Stain Set, Dade Diagnostics, Aguada, PR). ..

Diff-Quik:

Article Title: Human intestinal myofibroblasts deposited collagen VI enhances adhesiveness for T cells – A novel mechanism for maintenance of intestinal inflammation
Article Snippet: In specific experiments, 5 ng/ml phorbol 12-myristate 13-acetate (PMA, Sigma, St. Louis, MO, USA) was added for 1 h. After 3 h at 37 °C, non-adherent T cells were removed by gentle aspiration and wells rinsed 3 times with Ca ++ - and Mg ++ -containing HBSS. .. T cells were either pre-labeled by calcein (Thermo Fisher Scientific, Waltham, MA, USA) or were stained after adhesion and fixation (Diff Quick Stain Set, Dade Diagnostics, Aguada, PR). ..



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RBM23 knockdown inhibits colon cancer cell growth and survival (A) Protein was extracted from the normal colon cell lines CCD-18Co and colon cancer cell lines (HCT116, HT29, LOVO, LS513, DLD-1, COLO205, HCT15) and quantified in equal amounts, and then the protein expression of RBM23 was detected by western blotting. (B) The mRNA expression level of RBM23 was measured by qRT-PCR in the normal colon cell line CCD-18Co and colon cancer cell lines (DLD-1, HCT15, HT29, HCT116). GAPDH was used as an internal control for normalization. (C) Western blot analysis was performed to measure the expression levels of c-Myc in HCT15 cells treated with control siRNA or RBM23 siRNA for 72 h. (D) HCT116 cells were treated with control siRNA or RBM23 siRNA #1, #2, #3 for 72 h. Protein expression levels of various factors were then analyzed by western blotting. (E) The effect of RBM23 deficiency on HCT116, a colon cancer cell line. HCT116 was transfected with 80 nM RBM23 siRNA and control siRNA, and cell viability was examined at 0 and 72 h of treatment. Cell viability was measured by CCK8 assay and optical density was measured by microplate reader at 450 nm. Data were normalized to the control siRNA group at 0 h (set as 100%). (F) The effect of RBM23 knockdown in colon cancer cells, HCT116, on cell proliferation. HCT116 cells were transfected with RBM23 siRNA (100 nM) and incubated for one week, and colonies were stained with <t>Diff</t> <t>Quick</t> solution. The colonies were counted and quantified. (G) Western blotting was performed to detect proteins extracted from HCT116 cells fractionated into nucleus and cytoplasm. Proteins from HCT116 cells transfected with RBM23 siRNA (100 nM) for 72 h were extracted and separated by NE-PER nuclear and cytoplasmic extraction kit into proteins extracted from the nucleus and cytoplasm. The proteins were then detected using western blotting. Student’s t -test: ***P < 0.001
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RBM23 knockdown inhibits colon cancer cell growth and survival (A) Protein was extracted from the normal colon cell lines CCD-18Co and colon cancer cell lines (HCT116, HT29, LOVO, LS513, DLD-1, COLO205, HCT15) and quantified in equal amounts, and then the protein expression of RBM23 was detected by western blotting. (B) The mRNA expression level of RBM23 was measured by qRT-PCR in the normal colon cell line CCD-18Co and colon cancer cell lines (DLD-1, HCT15, HT29, HCT116). GAPDH was used as an internal control for normalization. (C) Western blot analysis was performed to measure the expression levels of c-Myc in HCT15 cells treated with control siRNA or RBM23 siRNA for 72 h. (D) HCT116 cells were treated with control siRNA or RBM23 siRNA #1, #2, #3 for 72 h. Protein expression levels of various factors were then analyzed by western blotting. (E) The effect of RBM23 deficiency on HCT116, a colon cancer cell line. HCT116 was transfected with 80 nM RBM23 siRNA and control siRNA, and cell viability was examined at 0 and 72 h of treatment. Cell viability was measured by CCK8 assay and optical density was measured by microplate reader at 450 nm. Data were normalized to the control siRNA group at 0 h (set as 100%). (F) The effect of RBM23 knockdown in colon cancer cells, HCT116, on cell proliferation. HCT116 cells were transfected with RBM23 siRNA (100 nM) and incubated for one week, and colonies were stained with Diff Quick solution. The colonies were counted and quantified. (G) Western blotting was performed to detect proteins extracted from HCT116 cells fractionated into nucleus and cytoplasm. Proteins from HCT116 cells transfected with RBM23 siRNA (100 nM) for 72 h were extracted and separated by NE-PER nuclear and cytoplasmic extraction kit into proteins extracted from the nucleus and cytoplasm. The proteins were then detected using western blotting. Student’s t -test: ***P < 0.001

Journal: Cancer Cell International

Article Title: Inhibition of RBM23 induces ferroptosis in colon cancer cells via c-Myc regulation

doi: 10.1186/s12935-026-04262-x

Figure Lengend Snippet: RBM23 knockdown inhibits colon cancer cell growth and survival (A) Protein was extracted from the normal colon cell lines CCD-18Co and colon cancer cell lines (HCT116, HT29, LOVO, LS513, DLD-1, COLO205, HCT15) and quantified in equal amounts, and then the protein expression of RBM23 was detected by western blotting. (B) The mRNA expression level of RBM23 was measured by qRT-PCR in the normal colon cell line CCD-18Co and colon cancer cell lines (DLD-1, HCT15, HT29, HCT116). GAPDH was used as an internal control for normalization. (C) Western blot analysis was performed to measure the expression levels of c-Myc in HCT15 cells treated with control siRNA or RBM23 siRNA for 72 h. (D) HCT116 cells were treated with control siRNA or RBM23 siRNA #1, #2, #3 for 72 h. Protein expression levels of various factors were then analyzed by western blotting. (E) The effect of RBM23 deficiency on HCT116, a colon cancer cell line. HCT116 was transfected with 80 nM RBM23 siRNA and control siRNA, and cell viability was examined at 0 and 72 h of treatment. Cell viability was measured by CCK8 assay and optical density was measured by microplate reader at 450 nm. Data were normalized to the control siRNA group at 0 h (set as 100%). (F) The effect of RBM23 knockdown in colon cancer cells, HCT116, on cell proliferation. HCT116 cells were transfected with RBM23 siRNA (100 nM) and incubated for one week, and colonies were stained with Diff Quick solution. The colonies were counted and quantified. (G) Western blotting was performed to detect proteins extracted from HCT116 cells fractionated into nucleus and cytoplasm. Proteins from HCT116 cells transfected with RBM23 siRNA (100 nM) for 72 h were extracted and separated by NE-PER nuclear and cytoplasmic extraction kit into proteins extracted from the nucleus and cytoplasm. The proteins were then detected using western blotting. Student’s t -test: ***P < 0.001

Article Snippet: The plates were then incubated at 37 °C, 5% CO 2 for 1 week and the colonies were fixed and stained using Diff-Quick Kit (Sysmex Corporation, Kobe, Hyogo, Japan) and the number of colonies was counted.

Techniques: Knockdown, Expressing, Western Blot, Quantitative RT-PCR, Control, Transfection, CCK-8 Assay, Incubation, Staining, Diff-Quik, Extraction