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HORIBA Ltd scientific openplex spr imaging (spri) instruments
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Scientific Openplex Spr Imaging (Spri) Instruments, supplied by HORIBA Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Siemens Healthineers spr prediction algorithm for image-based dect
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Spr Prediction Algorithm For Image Based Dect, supplied by Siemens Healthineers, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carterra Inc array-based spr imaging system
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Array Based Spr Imaging System, supplied by Carterra Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biacore spr imaging instrument biacore flexchip
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Spr Imaging Instrument Biacore Flexchip, supplied by Biacore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carterra Inc array-based spr imaging system cfm/ibis
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Array Based Spr Imaging System Cfm/Ibis, supplied by Carterra Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carterra Inc ibis mx96 spr imager (spri)
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Ibis Mx96 Spr Imager (Spri), supplied by Carterra Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Mendeley Ltd raw image, spr and stopped-flow data
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Raw Image, Spr And Stopped Flow Data, supplied by Mendeley Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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HORIBA Ltd sprilab spr imager
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Sprilab Spr Imager, supplied by HORIBA Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Varian Medical spr images
a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the <t>OpenPleX.</t> The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .
Spr Images, supplied by Varian Medical, 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/result/spr images/product/Varian Medical
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Image Search Results


a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the OpenPleX. The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .

Journal: Communications Biology

Article Title: Multiplexed proteomic biosensor platform for label-free real-time simultaneous kinetic screening of thousands of protein interactions

doi: 10.1038/s42003-025-07844-z

Figure Lengend Snippet: a Image of the SPOC sensor surface (10 k pattern) as viewed from the flowcell of the OpenPleX. The hockey-stick shaped orientation mark is visible in the center of the array. b Difference image showing the pattern of binding observed on the SPOC biosensor surface after injection of mouse anti-HaloTag antibody (133 nM). c Difference image showing the pattern of binding observed after the Mouse anti-Jun antibody injection (200 nM) which specifically detects two spots (yellow marks) where Jun-HaloTag was capture-purified as expected. d 1:1 fit (orange line) OpenPleX data of the anti-Jun antibody binding to Jun Spots #1 and #2 from c show similar binding profiles and equilibrium dissociation constants. e Difference image shows the pattern of binding observed after the mouse anti-p53 antibody injection (17.8 nM) which specifically detects four spots (yellow marks) where p53-HaloTag was capture-purified as expected. f 1:1 fit (orange lines) OpenPleX data of the anti-p53 antibody binding to the four p53 spots detected in e show similar binding profiles and equilibrium dissociation constants. g Iso-affinity plot of the kinetics measured for the Mouse anti-p53 and anti-Jun injections (p53 = 10 spots across 3 sensors; Jun = 4 spots across 2 sensors). The numerical source dataset for this iso-affinity plot is on Table .

Article Snippet: The SPOC technology is adaptable to any SPR instrument; however, for this publication, the custom Carterra LSA XT SPR and Horiba Scientific OpenPleX SPR imaging (SPRi) instruments were used for validation because both instruments are amenable to HTP screening and require minimal effort to integrate with our SPOC protein biosensor platform.

Techniques: Binding Assay, Injection, Purification

10 k SPOC array kinetic parameters derived from two protein specific antibody analytes binding to their respective target protein-ligands as measured on the  OpenPleX  instrument

Journal: Communications Biology

Article Title: Multiplexed proteomic biosensor platform for label-free real-time simultaneous kinetic screening of thousands of protein interactions

doi: 10.1038/s42003-025-07844-z

Figure Lengend Snippet: 10 k SPOC array kinetic parameters derived from two protein specific antibody analytes binding to their respective target protein-ligands as measured on the OpenPleX instrument

Article Snippet: The SPOC technology is adaptable to any SPR instrument; however, for this publication, the custom Carterra LSA XT SPR and Horiba Scientific OpenPleX SPR imaging (SPRi) instruments were used for validation because both instruments are amenable to HTP screening and require minimal effort to integrate with our SPOC protein biosensor platform.

Techniques: Derivative Assay, Binding Assay