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GenTel BioSurfaces sim plex 16 multi-array system device
Sim Plex 16 Multi Array System Device, supplied by GenTel BioSurfaces, 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/multi-array+system/simplex+16+multi+array+device/pmc03562209-150-8-14
Average 90 stars, based on 1 article reviews
sim plex 16 multi-array system device - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

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Article Title: Identification of proteins binding coding and non-coding human RNAs using protein microarrays
Article Snippet: The microarray slide was assembled in a Gentel SIM plex 16 Multi-Array System device (Gentel biosciences, cat# 4–1007) with custom modifications including a modified bottom gasket and top spacers (Additional file : Figure S1A).

Article Title: Deubiquitylase, DeSUMOylase, and DeISGylase Activity Microarrays for Assay of Substrate Preference and Functional Modifiers
Article Snippet: Arrays were then placed into GenTel's SIMplex 16-Multi Array system (catalogue #4-1001).

Article Title: A straightforward protocol for the preparation of high performance microarray displaying synthetic MUC1 glycopeptides.
Article Snippet: Hybridization covers (60 × 25 × 0.7 mm) were also obtained from Sumitomo Bakelite Co., Ltd. SIMplex 16 multi-array systemwas from GenTel BioSciences, Inc. (Madison, WI, USA).

Article Title: SCD fingerprints
Article Snippet: Reagents and Materials include 1× GenTel Wash Buffer, 1× GenTel Rinse Buffer, 1× GenTel Protein Free Blocking Buffer, 5× GenTel Print Buffer, GenTel PATHplus Thin Film Nitrocellulose Slides, GenTel SIMplex 16/64 Well Separator Device, Monoclonal Capture Antibodies, Recombinant Antigen standards, Detector Antibodies, and Streptavidin/Dy549.

Article Title: Cancer-related glycopeptide epitopes, antibodies and methods of use
Article Snippet: Set the Microarray slide in SIMprex 64 Multi-Array Device (Gentel Biosciences, #4-1029) with SIMprex Gasket (Gentel Biosciences, #4-1026).

Centrifugation:

Article Title: Clinical utility of serum autoantibodies detected by protein microarray in melanoma.
Article Snippet: The slides were washed three times with 0.1% Tween20 in PBS buffer (PBST) and then blocked with 1% bovine serum albumin (Roche) in PBST for 1 hr. .. The blocked slides were dried by centrifugation and inserted into a SIMplex (Gentel Bioscience) multiarray device which divides each slide by 16 wells. ..

Modification:

Article Title: Identification of proteins binding coding and non-coding human RNAs using protein microarrays
Article Snippet: .. Coding RNA SO X2 OT _a nti se ns e SO X2 OT _s en se PW RN 1_ an tis en se OC C1 _s en se lin cR BM 26 _a nti se ns e lin cR BM 26 _s en se DL EU 1_ se ns e TP 53 _s en se OC C1 _a nti se ns e HR AS _s en se MY C_ an tis en se MY C_ se ns e HR AS _a nti se ns e BC L2 _s en se BC L2 _a nti se ns e IG F2 RN C_ an tis en se IG F2 RN C_ se ns e DL EU 1_ an tis en se PW RN 1_ se ns e TP 53 _a nti se ns e M Non-coding RNA D Bi ot in16 -U TP -T P5 3_ se ns e M Bi ot in16 -U TP -H RA S_ se ns e Bi ot in16 -U TP -L ac Z_ se ns e C 65 m m 25 mm 3 mm 2.5 mm 2.5 mm 3 mm 4 mm Top View Side View Gasket 22 mm 22 mm 5 m m 12 m m 1 mm 1 mm Top View Side View Spacer To p S pa ce r B ot to m S pa ce r Modified Gentel SIMplex 16 Device Bottom Piece Top Piece Top Spacer Bottom Spacer Fully Assembled Gasket ProtoArray Slide ..



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(A) Representative image of multi-unit recordings setup of ex vivo thalamic horizontal slices in a humidified, oxygenated interface chamber. (B) Schematic of multi-unit activity recordings with a Neuronexus 16-channel recording electrode positioned in the thalamus following electrical stimulation of the internal capsule. (C) Representative 3-second recording of intrathalamic multi-unit activity evoked by stimulation of the internal capsule (black dot indicates time of stimulation). Only 12 of 16 channels are shown for clarity. (D) Collapsed activity from 12 recording channels in (C). Black dot indicates time of stimulation. (E) Post-stimulus time histogram of instantaneous spiking frequency from multi-unit activity recorded across 16 channels (all 16 channels were analyzed, 12 representative channels are displayed in (C) from 15 slices from 9 hCSF1 (WT) mice, 8 slices from 7 hCSF1-Grn −/− +KOxMG mice, and 12 slices from 9 hCSF1-Grn −/− +WTxMG mice. The grey box denotes early response (0–1.5 s), and the white box denotes delayed response (1.5–3 s) after stimulation. (F) Enlarged instantaneous frequency of the delayed response (1.5–3 s) from (D). (G) Relative probability of eliciting spiking during the direct response (0–1.5 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (* p = 0.0024). (H) Instantaneous frequency of spiking during the early response (0–1.5 s) after stimulation; Kruskal–Wallis test, H(3) = 6.767, p = 0.0797. (I) Relative probability of eliciting spiking during the delayed response (1.5–3 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (**** p < 0.0001). (J) Instantaneous frequency of spiking during the delayed response (1.5–3 s) after stimulation; Kruskal-Wallis test, H(3)=56.6, **** p < 0.0001, and Dunn’s multiple comparisons test (**** p < 0.0001). Data are presented as mean ± SEM. Comparisons not shown are not significant.

Journal: bioRxiv

Article Title: Transplantation of Human IPSC-derived Microglia Ameliorates Neuropathology and Circuit Dysfunction in Progranulin-Deficient Mice

doi: 10.64898/2026.01.13.699312

Figure Lengend Snippet: (A) Representative image of multi-unit recordings setup of ex vivo thalamic horizontal slices in a humidified, oxygenated interface chamber. (B) Schematic of multi-unit activity recordings with a Neuronexus 16-channel recording electrode positioned in the thalamus following electrical stimulation of the internal capsule. (C) Representative 3-second recording of intrathalamic multi-unit activity evoked by stimulation of the internal capsule (black dot indicates time of stimulation). Only 12 of 16 channels are shown for clarity. (D) Collapsed activity from 12 recording channels in (C). Black dot indicates time of stimulation. (E) Post-stimulus time histogram of instantaneous spiking frequency from multi-unit activity recorded across 16 channels (all 16 channels were analyzed, 12 representative channels are displayed in (C) from 15 slices from 9 hCSF1 (WT) mice, 8 slices from 7 hCSF1-Grn −/− +KOxMG mice, and 12 slices from 9 hCSF1-Grn −/− +WTxMG mice. The grey box denotes early response (0–1.5 s), and the white box denotes delayed response (1.5–3 s) after stimulation. (F) Enlarged instantaneous frequency of the delayed response (1.5–3 s) from (D). (G) Relative probability of eliciting spiking during the direct response (0–1.5 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (* p = 0.0024). (H) Instantaneous frequency of spiking during the early response (0–1.5 s) after stimulation; Kruskal–Wallis test, H(3) = 6.767, p = 0.0797. (I) Relative probability of eliciting spiking during the delayed response (1.5–3 s) after stimulation; p values from Kolmogorov-Smirnov test with Bonferroni correction (**** p < 0.0001). (J) Instantaneous frequency of spiking during the delayed response (1.5–3 s) after stimulation; Kruskal-Wallis test, H(3)=56.6, **** p < 0.0001, and Dunn’s multiple comparisons test (**** p < 0.0001). Data are presented as mean ± SEM. Comparisons not shown are not significant.

Article Snippet: Extracellular multi-unit activity (MUA) recordings were obtained with a linear 16-channel multi-electrode array (Neuronexus) that spanned the nRT and VB thalamic regions.

Techniques: Ex Vivo, Activity Assay