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Bangs Laboratories quantumtm alexa fluor® 647 mesf microsphere kit
Quantumtm Alexa Fluor® 647 Mesf Microsphere Kit, supplied by Bangs Laboratories, 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/quantumtm+mesf+kit/quantum+alexa+fluor+647+mesf+beads/10__1158_slash_1078___0432__ccr___24___3083-86-9-16
Average 90 stars, based on 1 article reviews
quantumtm alexa fluor® 647 mesf microsphere kit - by Bioz Stars, 2026-09
90/100 stars

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other:

Article Title: Bortezomib alleviates antibody-mediated rejection in kidney transplantation by facilitating Atg5 expression.
Article Snippet: The QuantumTM MESF Kit (Bangs Laboratories) is supplied with one blank microsphere population and four microsphere populations that are surface- labelled with increasing concentrations of a specified fluorochrome.

Article Title: (F)Utility of the physical crossmatch for living donor evaluations in the age of the virtual crossmatch.
Article Snippet: Flow cytometric crossmatches (FCXM) are routinely performed to support living-donor renal transplantation.. While long a laboratory mainstay, a physical crossmatch is costly, time consuming, and frequently poses interpretative conundrums with both false-positive and false negative results.. Given the increased utilization of the virtual crossmatch (vXM) in the deceased donor setting, our aim was to assess its utility in living donor evaluations.

Labeling:

Article Title: A trypanosome-derived immunotherapeutics platform elicits potent high-affinity antibodies, negating the effects of the synthetic opioid fentanyl.
Article Snippet: .. For the standard curve, the QuantumTM MESF kit was obtained from Bangs Laboratories, containing one blank bead population and a series of five fluorescent bead populations labeled with varying amounts of FITC. ..

Fluorescence:

Article Title: Hiding in plain sight: Misinterpretation of immunogenic DPB epitopes within G/P groups. Short running title: The impact of HLA G and P codes on DPB.
Article Snippet: The clinical impact of HLA DP antibodies is poorly understood, resulting in variable clinical strategies for transplant candidates and recipients with donor‐directed HLA‐DP antibodies.. Complicating matters further, the DPB naming convention is not based on allelic homology and requires sequence alignments to identify potential immunogenic epitopes.. Historically, G and P codes, which consolidated alleles that were identical over Exon 2, were used to simplify the reporting of HLA Class II typing as differences outside of Exon 2 have not been considered immunogenic (i.e., able to induce an antibody response).

Article Title: Quantitative Flow Cytometry to Measure Viral Production Using Infectious Pancreatic Necrosis Virus as a Model: A Preliminary Study
Article Snippet: .. Fluorescence parameters (in terms of arbitrary fluorescence intensity; AFI) were standardised in Molecules of Equivalent Soluble Fluorochrome (MESF) units by means of type IIIb standard microsphere beads [29] using a QuantumTM MESF Kit (Bangs Laboratories, Inc., Burlington, ON, Canada). ..



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The glycosylation of EphB2 is indispensable for ephrin-A5/B2 binding specificity (A) Top: western blot and Coomassie brilliant blue staining results of purified EphB2 protein before/after PNGase F treatment. Bottom: western blot results of endogenous EphB2 from adult and P10 mice hippocampus before/after PNGase F enzyme treatment. GAPDH served as a loading control. (B) Flow diagram of FCM assay. EphB2-expressing cells bound by pre-clustered ephrin-A5 or ephrin-B2 were recorded by flow cytometry and translated to the relative <t>MESF</t> values. (C) The FCM results are analyzed by the “one-site specific binding” model to fit the saturation binding curves and obtain the K D values. The K D of EphB2 WT to ephrin-B2 and ephrin-A5 are 3.526 nM and 111.9 nM; the K D of EphB2 4Q to ephrin-B2 and ephrin-A5 are 29.91 nM and 32.29 nM. (D and E) Representative confocal microscopy images of ligand-induced ligand/receptor colocalization assays upon stimulating with ephrin ligands. Green represents cells expressing EphB2 4Q, and red represents 647-labeled pre-clustered ephrin ligands. Scale bar: 10 μm. Averaged ratios of cells with EphB2 4Q/ephrins colocalization after stimulation are plotted as (E). Statistical significance was performed by two-way ANOVA; Tukey’s post-hoc multiple comparisons test; ns, not significant; ( n = 3). (F) Representative western blot results of immunoprecipitated C-terminal 3 × FLAG EphB2 WT or EphB2 4Q in HEK293T cells after ephrin-A5 or ephrin-B2 stimulation. (G) Measurement of relative EphB2 tyrosine phosphorylation, correlated with (F). Statistical significance was performed by one-way ANOVA; Tukey’s post-hoc multiple comparisons test, ns, not significant; ∗ p < 0.05; ∗∗ p < 0.01; ( n = 3). All data are represented as mean ± SD.
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The glycosylation of EphB2 is indispensable for ephrin-A5/B2 binding specificity (A) Top: western blot and Coomassie brilliant blue staining results of purified EphB2 protein before/after PNGase F treatment. Bottom: western blot results of endogenous EphB2 from adult and P10 mice hippocampus before/after PNGase F enzyme treatment. GAPDH served as a loading control. (B) Flow diagram of FCM assay. EphB2-expressing cells bound by pre-clustered ephrin-A5 or ephrin-B2 were recorded by flow cytometry and translated to the relative MESF values. (C) The FCM results are analyzed by the “one-site specific binding” model to fit the saturation binding curves and obtain the K D values. The K D of EphB2 WT to ephrin-B2 and ephrin-A5 are 3.526 nM and 111.9 nM; the K D of EphB2 4Q to ephrin-B2 and ephrin-A5 are 29.91 nM and 32.29 nM. (D and E) Representative confocal microscopy images of ligand-induced ligand/receptor colocalization assays upon stimulating with ephrin ligands. Green represents cells expressing EphB2 4Q, and red represents 647-labeled pre-clustered ephrin ligands. Scale bar: 10 μm. Averaged ratios of cells with EphB2 4Q/ephrins colocalization after stimulation are plotted as (E). Statistical significance was performed by two-way ANOVA; Tukey’s post-hoc multiple comparisons test; ns, not significant; ( n = 3). (F) Representative western blot results of immunoprecipitated C-terminal 3 × FLAG EphB2 WT or EphB2 4Q in HEK293T cells after ephrin-A5 or ephrin-B2 stimulation. (G) Measurement of relative EphB2 tyrosine phosphorylation, correlated with (F). Statistical significance was performed by one-way ANOVA; Tukey’s post-hoc multiple comparisons test, ns, not significant; ∗ p < 0.05; ∗∗ p < 0.01; ( n = 3). All data are represented as mean ± SD.

Journal: iScience

Article Title: Ligand preference of EphB2 receptor is selectively regulated by N-glycosylation

doi: 10.1016/j.isci.2025.112386

Figure Lengend Snippet: The glycosylation of EphB2 is indispensable for ephrin-A5/B2 binding specificity (A) Top: western blot and Coomassie brilliant blue staining results of purified EphB2 protein before/after PNGase F treatment. Bottom: western blot results of endogenous EphB2 from adult and P10 mice hippocampus before/after PNGase F enzyme treatment. GAPDH served as a loading control. (B) Flow diagram of FCM assay. EphB2-expressing cells bound by pre-clustered ephrin-A5 or ephrin-B2 were recorded by flow cytometry and translated to the relative MESF values. (C) The FCM results are analyzed by the “one-site specific binding” model to fit the saturation binding curves and obtain the K D values. The K D of EphB2 WT to ephrin-B2 and ephrin-A5 are 3.526 nM and 111.9 nM; the K D of EphB2 4Q to ephrin-B2 and ephrin-A5 are 29.91 nM and 32.29 nM. (D and E) Representative confocal microscopy images of ligand-induced ligand/receptor colocalization assays upon stimulating with ephrin ligands. Green represents cells expressing EphB2 4Q, and red represents 647-labeled pre-clustered ephrin ligands. Scale bar: 10 μm. Averaged ratios of cells with EphB2 4Q/ephrins colocalization after stimulation are plotted as (E). Statistical significance was performed by two-way ANOVA; Tukey’s post-hoc multiple comparisons test; ns, not significant; ( n = 3). (F) Representative western blot results of immunoprecipitated C-terminal 3 × FLAG EphB2 WT or EphB2 4Q in HEK293T cells after ephrin-A5 or ephrin-B2 stimulation. (G) Measurement of relative EphB2 tyrosine phosphorylation, correlated with (F). Statistical significance was performed by one-way ANOVA; Tukey’s post-hoc multiple comparisons test, ns, not significant; ∗ p < 0.05; ∗∗ p < 0.01; ( n = 3). All data are represented as mean ± SD.

Article Snippet: Quantumtm MESF microsphere kits , Bangs Laboratories , PSD818.

Techniques: Glycoproteomics, Binding Assay, Western Blot, Staining, Purification, Control, Expressing, Flow Cytometry, Confocal Microscopy, Labeling, Immunoprecipitation, Phospho-proteomics

Journal: iScience

Article Title: DAP12-associated synthetic antigen receptors enable multi-targeting of T cells with independent chimeric receptors in a small genetic payload

doi: 10.1016/j.isci.2025.112142

Figure Lengend Snippet:

Article Snippet: QuantumTM Alexa Fluor® 647 MESF kit , Bangs Laboratories , Cat# 647.

Techniques: FLAG-tag, Control, Virus, Generated, Subcloning, Recombinant, Staining, Flow Cytometry, Selection, Gene Knockout, Plasmid Preparation, Cloning, Expressing, Software