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snap surface alexa fluor 647  (New England Biolabs)


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    New England Biolabs snap surface alexa fluor 647
    Snap Surface Alexa Fluor 647, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 356 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/snap-surface+alexa+fluor+647/SNAP-Surface+Alexa+Fluor+647/pm42814554-310-6-11
    Average 97 stars, based on 356 article reviews
    snap surface alexa fluor 647 - by Bioz Stars, 2026-10
    97/100 stars

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    Article Snippet: PrePrint: , and strong irritant that poses risks to human health upon contact, inhalation, or ingestion, potentially causing skin, eye, and respiratory irritation, as well as sensitization and allergic reactions. SNAP-Surface BG-AF647 (New England Biolabs, cat. no. S9136S) Bovine Serum Albumin (BSA, Sigma-Aldrich, cat. No. A7030) Catalase (Sigma-Aldrich, cat. No. C3155) Isopropanol (Merck, cat. no. 67-63-0). CAUTION: Handle with care. Isopropanol is highly



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    ( A ) Cartoon showing the CaSR cytoplasmic region for the WT and 895X truncation plasmid. The Thr888 residue that has previously been shown to have a critical role in CaSR signalling is highlighted and was retained in the truncation plasmid. ( B ) Confocal images of the CaSR-WT and CaSR-895X plasmids in HEK-βarr1/2 KO cells. ( C ) Assessment of cell surface expression measured by labelling surface receptor with a CaSR antibody and a secondary Alexa <t>Fluor</t> <t>647</t> antibody. Fluorescence was normalized to cells expressing CaSR-WT. ( D ) Ca 2+ i responses measured by fluo-4 with ( E ) EC 50 in cells transfected with CaSR WT or 895X. ( F ) βarrestin-1 (N=9) and ( G ) βarrestin-2 (N=9) recruitment to CaSR in cells expressing CaSR WT and 895X plasmids. AUC was measured to derive concentration-response curves. Statistical analyses were performed by two-way ANOVA with Sidak’s multiple-comparisons test. *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.
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    ( A ) Cartoon showing the CaSR cytoplasmic region for the WT and 895X truncation plasmid. The Thr888 residue that has previously been shown to have a critical role in CaSR signalling is highlighted and was retained in the truncation plasmid. ( B ) Confocal images of the CaSR-WT and CaSR-895X plasmids in HEK-βarr1/2 KO cells. ( C ) Assessment of cell surface expression measured by labelling surface receptor with a CaSR antibody and a secondary Alexa <t>Fluor</t> <t>647</t> antibody. Fluorescence was normalized to cells expressing CaSR-WT. ( D ) Ca 2+ i responses measured by fluo-4 with ( E ) EC 50 in cells transfected with CaSR WT or 895X. ( F ) βarrestin-1 (N=9) and ( G ) βarrestin-2 (N=9) recruitment to CaSR in cells expressing CaSR WT and 895X plasmids. AUC was measured to derive concentration-response curves. Statistical analyses were performed by two-way ANOVA with Sidak’s multiple-comparisons test. *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.
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    ( A ) Cartoon showing the CaSR cytoplasmic region for the WT and 895X truncation plasmid. The Thr888 residue that has previously been shown to have a critical role in CaSR signalling is highlighted and was retained in the truncation plasmid. ( B ) Confocal images of the CaSR-WT and CaSR-895X plasmids in HEK-βarr1/2 KO cells. ( C ) Assessment of cell surface expression measured by labelling surface receptor with a CaSR antibody and a secondary Alexa <t>Fluor</t> <t>647</t> antibody. Fluorescence was normalized to cells expressing CaSR-WT. ( D ) Ca 2+ i responses measured by fluo-4 with ( E ) EC 50 in cells transfected with CaSR WT or 895X. ( F ) βarrestin-1 (N=9) and ( G ) βarrestin-2 (N=9) recruitment to CaSR in cells expressing CaSR WT and 895X plasmids. AUC was measured to derive concentration-response curves. Statistical analyses were performed by two-way ANOVA with Sidak’s multiple-comparisons test. *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.
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    ( A ) Cartoon showing the CaSR cytoplasmic region for the WT and 895X truncation plasmid. The Thr888 residue that has previously been shown to have a critical role in CaSR signalling is highlighted and was retained in the truncation plasmid. ( B ) Confocal images of the CaSR-WT and CaSR-895X plasmids in HEK-βarr1/2 KO cells. ( C ) Assessment of cell surface expression measured by labelling surface receptor with a CaSR antibody and a secondary Alexa <t>Fluor</t> <t>647</t> antibody. Fluorescence was normalized to cells expressing CaSR-WT. ( D ) Ca 2+ i responses measured by fluo-4 with ( E ) EC 50 in cells transfected with CaSR WT or 895X. ( F ) βarrestin-1 (N=9) and ( G ) βarrestin-2 (N=9) recruitment to CaSR in cells expressing CaSR WT and 895X plasmids. AUC was measured to derive concentration-response curves. Statistical analyses were performed by two-way ANOVA with Sidak’s multiple-comparisons test. *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.
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    Image Search Results


    ( A ) Cartoon showing the CaSR cytoplasmic region for the WT and 895X truncation plasmid. The Thr888 residue that has previously been shown to have a critical role in CaSR signalling is highlighted and was retained in the truncation plasmid. ( B ) Confocal images of the CaSR-WT and CaSR-895X plasmids in HEK-βarr1/2 KO cells. ( C ) Assessment of cell surface expression measured by labelling surface receptor with a CaSR antibody and a secondary Alexa Fluor 647 antibody. Fluorescence was normalized to cells expressing CaSR-WT. ( D ) Ca 2+ i responses measured by fluo-4 with ( E ) EC 50 in cells transfected with CaSR WT or 895X. ( F ) βarrestin-1 (N=9) and ( G ) βarrestin-2 (N=9) recruitment to CaSR in cells expressing CaSR WT and 895X plasmids. AUC was measured to derive concentration-response curves. Statistical analyses were performed by two-way ANOVA with Sidak’s multiple-comparisons test. *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.

    Journal: bioRxiv

    Article Title: Loss of phosphorylation sites required for β-arrestin recruitment in the calcium-sensing receptor cytoplasmic region may contribute to hypocalcemia

    doi: 10.64898/2026.04.21.719673

    Figure Lengend Snippet: ( A ) Cartoon showing the CaSR cytoplasmic region for the WT and 895X truncation plasmid. The Thr888 residue that has previously been shown to have a critical role in CaSR signalling is highlighted and was retained in the truncation plasmid. ( B ) Confocal images of the CaSR-WT and CaSR-895X plasmids in HEK-βarr1/2 KO cells. ( C ) Assessment of cell surface expression measured by labelling surface receptor with a CaSR antibody and a secondary Alexa Fluor 647 antibody. Fluorescence was normalized to cells expressing CaSR-WT. ( D ) Ca 2+ i responses measured by fluo-4 with ( E ) EC 50 in cells transfected with CaSR WT or 895X. ( F ) βarrestin-1 (N=9) and ( G ) βarrestin-2 (N=9) recruitment to CaSR in cells expressing CaSR WT and 895X plasmids. AUC was measured to derive concentration-response curves. Statistical analyses were performed by two-way ANOVA with Sidak’s multiple-comparisons test. *p<0.05, **p<0.01, ***p<0.001, ****p<0.0001.

    Article Snippet: On the day of the experiment SNAP-Surface Alexa Fluor 647 (NEB) was diluted 1:1000 in FluoroBrite complete media and applied to cells for 20-minutes, before washing and imaging.

    Techniques: Plasmid Preparation, Residue, Expressing, Fluorescence, Transfection, Concentration Assay

    ( A ) SIM of HA-SNAP-CaSR (labelled with the HA antibody and an Alexa Fluor 647 secondary antibody) and Venus-Kras in AdHEK cells. Scale, 5μm. ( B ) Western blot analyses to detect CaSR in cells transfected with mock (pcDNA3.1), FLAG-CaSR-WT (FLAG) and HA-SNAP-CaSR-WT (CaSR) plasmids showing similar expression levels. Calnexin was used as a loading control. The blot shows lysates from three independent transfections. ( C ) Normalized Ca 2+ i signaling measured by Fluo-4 assays. N=5 biological replicates. The maximal response for each drug concentration was derived and normalized to baseline responses of the CaSR-WT transfected wells to derive the concentration-response curve. ( D ) IP-1 responses in cells transfected with HA-SNAP-CaSR and FLAG-CaSR. N=3 biological replicates. ( E ) SIM images of HA-SNAP-CaSR exposed to 5mM Ca 2+ e and the HA antibody for 0 or 30 minutes.

    Journal: bioRxiv

    Article Title: Loss of phosphorylation sites required for β-arrestin recruitment in the calcium-sensing receptor cytoplasmic region may contribute to hypocalcemia

    doi: 10.64898/2026.04.21.719673

    Figure Lengend Snippet: ( A ) SIM of HA-SNAP-CaSR (labelled with the HA antibody and an Alexa Fluor 647 secondary antibody) and Venus-Kras in AdHEK cells. Scale, 5μm. ( B ) Western blot analyses to detect CaSR in cells transfected with mock (pcDNA3.1), FLAG-CaSR-WT (FLAG) and HA-SNAP-CaSR-WT (CaSR) plasmids showing similar expression levels. Calnexin was used as a loading control. The blot shows lysates from three independent transfections. ( C ) Normalized Ca 2+ i signaling measured by Fluo-4 assays. N=5 biological replicates. The maximal response for each drug concentration was derived and normalized to baseline responses of the CaSR-WT transfected wells to derive the concentration-response curve. ( D ) IP-1 responses in cells transfected with HA-SNAP-CaSR and FLAG-CaSR. N=3 biological replicates. ( E ) SIM images of HA-SNAP-CaSR exposed to 5mM Ca 2+ e and the HA antibody for 0 or 30 minutes.

    Article Snippet: On the day of the experiment SNAP-Surface Alexa Fluor 647 (NEB) was diluted 1:1000 in FluoroBrite complete media and applied to cells for 20-minutes, before washing and imaging.

    Techniques: Western Blot, Transfection, Expressing, Control, Concentration Assay, Derivative Assay