Review

diff-quick kit (Medion Diagnostics)

About

News

Press Release

Team

Advisors

Partners

Contact

Bioz Stars

Bioz vStars

Buy from Supplier

Structured Review

Medion Diagnostics diff-quick kit
Diff Quick Kit, supplied by Medion Diagnostics, 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/diff-quick+kit/diff+quick+kit/pm31042078-81-31-33
Average 90 stars, based on 1 article reviews

diff-quick kit - by Bioz Stars, 2026-09

90/100 stars

Images

Staining:

Article Title: Kinematic and Morphometric Assessment of Fresh Semen, before, during and after Mating Period in Brahman Bulls
Article Snippet: Samples were stained with the Diff-Quick ® commercial kit (Medion Diagnostics, Düdingen, Switzerland), according to the manufacturer’s instructions.

Article Title: MUC1 Drives the Progression and Chemoresistance of Clear Cell Renal Carcinomas.
Article Snippet: Then, the cells located on the lower surface of the chamber were fixed with the Diff-Quick kit (Medion Diagnostics, Düdingen, Germany), stained with DAPI, and counted.

Article Title: Ameliorative effects of Myrtus communis L. extract involving the inhibition of oxidative stress on high fat diet-induced testis damage in rats.
Article Snippet: The possible protective effects of Myrtus communis L. (MC) extract on a high fat diet (HFD)induced testicular injury in a rat model were investigated using histological and biochemical methods.. Wistar albino rats were divided into three groups: a standard diet control group; a HFD group; and an HFD+MC group.. The HFD and HFD+MC groups were fed with a HFD for 16 weeks.

Article Title: Apocynin Ameliorates Monosodium Glutamate Induced Testis Damage by Impaired Blood-Testis Barrier and Oxidative Stress Parameters.
Article Snippet: For morphological evaluation, smears were prepared and then stained using the Diff-Quick kit (Medion Diagnostics, Grafelfing, Munich, Germany).

Article Title: Per- and polyfluoroalkyl substances (PFAS) in little penguins and associations with urbanisation and health parameters.
Article Snippet: To assess circulating blood cells, one of the blood slides obtained in the field was stained using the RomanowskyTM technique and a Diff-Quick kit (Medion Diagnostics GmbH, Düdingen, Germany).

Article Title: Candesartan Mediated Amelioration of Cisplatin-Induced Testicular Damage Is Associated with Alterations in Expression Patterns of Nephrin and Podocin
Article Snippet: In order to detect the spermatozoa with abnormal morphologies, the Diff-Quick kit (Medion Diagnostics International, FL, USA) was used to stain the smears of semen samples.

Article Title: Kinematic and Morphometric Assessment of Fresh Semen, before, during and after Mating Period in Brahman Bulls.
Article Snippet: Samples were stained with the Diff-Quick® commercial kit (Medion Diagnostics, Düdingen, Switzerland), according to the manufacturer’s instructions.

Article Title: Flow cytometric analysis of the leukocyte landscape during bleomycin-induced lung injury and fibrosis in the rat.
Article Snippet: The different cell populations were sorted following the same gating strategy, combining the 176 antibodies CD45-PE, CD11b/c-APC-Vio770, CD163-FITC, MHC-II-VioBlue and α-granulocyte-APC, spun 177 down into slides and differentially stained using the Diff-Quick kit (Medion Diagnostics, Miami, FL, 178 USA) following manufacturer ́s instructions.

Diff-Quik:

Immunopeptidomics:

Similar Products

Image Search Results

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

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