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streptavidin conjugated alexa 647  (Thermo Fisher)


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    Structured Review

    Thermo Fisher streptavidin conjugated alexa 647
    Streptavidin Conjugated Alexa 647, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/microarray+blocking+solution/Streptavidin/ppr0055369-104-7-10
    Average 99 stars, based on 1 article reviews
    streptavidin conjugated alexa 647 - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Protein Concentration:

    Article Title: OT-Curtains: an approach for studying protein interactions with DNA ends using optical tweezers and confocal fluorescence microscopy
    Article Snippet: .. In some experiments, bio-AddAB was pre-incubated with streptavidin-conjugated Qdot525 (Thermo Fisher Scientific, Q10143MP) at a 1:2 (AddAB:Qdot) molar ratio for 10 min on ice before dilution with experimental buffer to a final protein concentration of 10 nM (referred to as QD525-AddAB). ..

    other:

    Article Title: Interacting proteins of AMPK studied using TurboID proximity labeling technology
    Article Snippet: Dynabeads MyOne streptavidin C1 (cat. no. 65001), biotin (cat. no. B20656 ) and liposomal transfection reagent (Lipofectamine 2000; cat. no. 11668500) were obtained from Thermo Fisher Scientific, Inc. RIPA buffer (cat. no. G2002-100ML), DAPI (cat. no. G1012-100ML) and anti-fluorescence quenching sealing agent (cat. no. G1401-25ML) were purchased from Wuhan Servicebio Technology Co., Ltd.

    Article Title: A conserved mammalian mecciRNA, mecciATP6, regulates mitochondrial homeostasis through interaction with HNRNPA3
    Article Snippet: For smFISH and immunofluorescence (IF) analyses, the colocalization ratio between smFISH/IF signals and mitochondria was quantified using the Coloc2 plugin in ImageJ.

    Article Title: Targeting Mettl8-Tcf1 axis promotes CD8 + T PEX differentiation and antitumor immunity
    Article Snippet: The DNA ends were blunted and labeled with biotin by Klenow DNA polymerase in the presence of dCTP, dGTP, dTTP, and biotin-14-dATP, followed by ligation using T4 DNA ligase (NEB).

    Transfection:

    Article Title: CircEif3c/miR-96–5p/PHF20L1/MEOX2 axis in perivascular preadipocyte exosomes mediates fibroblast dysfunction and vascular remodeling
    Article Snippet: Biotin-labeled miRNAs were transfected into cells using Lipofectamine 3000 (#L3000-001, Invitrogen, Thermo Fisher Scientific, USA), and cell lysates were subsequently collected. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR.

    Incubation:

    Article Title: CircEif3c/miR-96–5p/PHF20L1/MEOX2 axis in perivascular preadipocyte exosomes mediates fibroblast dysfunction and vascular remodeling
    Article Snippet: Biotin-labeled miRNAs were transfected into cells using Lipofectamine 3000 (#L3000-001, Invitrogen, Thermo Fisher Scientific, USA), and cell lysates were subsequently collected. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR.

    Article Title: HSF1 and YTHDC1 enhance DNA repair under heat stress by promoting repair-associated gene expression
    Article Snippet: The samples were washed three more times in PBS containing 0.1% Tween 20, incubated with 4′,6-diamidino-2-phenylindole (DAPI) (1 μg/ml, Beyotime, C1002) for 5 min, and sealed. .. In addition, cells were incubated with streptavidin 488 (Invitrogen, S11223 ) simultaneously with secondary antibodies. .. Images were acquired using a Leica STELLARIS 5 microscope or a Leica TCS SP8 STED 3X microscope for high-resolution STED imaging.

    Article Title: CircSMAD4 shapes matrix-remodeling TAMs in lung adenocarcinoma
    Article Snippet: Samples were acquired on a BD LSRFortessa flow cytometer. .. Biotinylated circSMAD4 sense RNA (with antisense RNA as a negative control) was generated by in vitro transcription using Biotin-16-UTP (Beyotime, Cat# D7336), incubated with macrophage lysates, and captured using streptavidin beads (Invitrogen, Cat# 88816). ..

    Magnetic Beads:

    Article Title: CircEif3c/miR-96–5p/PHF20L1/MEOX2 axis in perivascular preadipocyte exosomes mediates fibroblast dysfunction and vascular remodeling
    Article Snippet: Biotin-labeled miRNAs were transfected into cells using Lipofectamine 3000 (#L3000-001, Invitrogen, Thermo Fisher Scientific, USA), and cell lysates were subsequently collected. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR.

    Centrifugation:

    Article Title: CircEif3c/miR-96–5p/PHF20L1/MEOX2 axis in perivascular preadipocyte exosomes mediates fibroblast dysfunction and vascular remodeling
    Article Snippet: Biotin-labeled miRNAs were transfected into cells using Lipofectamine 3000 (#L3000-001, Invitrogen, Thermo Fisher Scientific, USA), and cell lysates were subsequently collected. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR. .. Cell lysates were collected 48 h after transfection and incubated with streptavidin magnetic beads (#65306, Invitrogen, USA) for 2 h. After centrifugation to wash the beads, the pulled-down miRNAs were extracted using Trizol (#15596018, Invitrogen, USA) and subjected to qRT-PCR.

    Cell-Signaling:

    Article Title: Divalent siRNA for prion disease
    Article Snippet: .. The assay uses antibodies EP1802Y (Abcam, ab52604) for capture and in-house biotinylated 8H4 (Abcam ab61409) for detection, followed by streptavidin–horseradish peroxidase (Thermo Fisher Scientific, 21130) and TMB (Cell Signaling, 7004P4). ..

    Negative Control:

    Article Title: CircSMAD4 shapes matrix-remodeling TAMs in lung adenocarcinoma
    Article Snippet: Samples were acquired on a BD LSRFortessa flow cytometer. .. Biotinylated circSMAD4 sense RNA (with antisense RNA as a negative control) was generated by in vitro transcription using Biotin-16-UTP (Beyotime, Cat# D7336), incubated with macrophage lysates, and captured using streptavidin beads (Invitrogen, Cat# 88816). ..

    Generated:

    Article Title: CircSMAD4 shapes matrix-remodeling TAMs in lung adenocarcinoma
    Article Snippet: Samples were acquired on a BD LSRFortessa flow cytometer. .. Biotinylated circSMAD4 sense RNA (with antisense RNA as a negative control) was generated by in vitro transcription using Biotin-16-UTP (Beyotime, Cat# D7336), incubated with macrophage lysates, and captured using streptavidin beads (Invitrogen, Cat# 88816). ..

    In Vitro:

    Article Title: CircSMAD4 shapes matrix-remodeling TAMs in lung adenocarcinoma
    Article Snippet: Samples were acquired on a BD LSRFortessa flow cytometer. .. Biotinylated circSMAD4 sense RNA (with antisense RNA as a negative control) was generated by in vitro transcription using Biotin-16-UTP (Beyotime, Cat# D7336), incubated with macrophage lysates, and captured using streptavidin beads (Invitrogen, Cat# 88816). ..



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    Gsk3 negatively regulates mitotic effectors in Xenopus extracts. (A) Scheme of the protein <t>microarray</t> experiment to assess Gsk3-dependent polyubiquitination. Interphase egg extracts were supplemented with ubiquitin, pretreated with LiCl or NaCl (Control), and then applied on protein arrays containing ∼9,000 proteins. Polyubiquitination of arrayed proteins (PolyUb) was monitored using anti-polyubiquitin antibodies and immunofluorescence detection using an array scanner. Signal intensities were transformed and are displayed as heat-map. (B) Distribution plot of polyubiquitination changes of 3,873 in vitro polyubiquitinated proteins after Gsk3 inhibition by LiCl (Log2[Control/LiCl]). Arrays were treated with 30 mM LiCl or 30 mM NaCl (Control). LiCl reduced polyubiquitination of 864 proteins >1.8-fold. Some candidates, associated with cell cycle progression and selected for further validation are indicated in the plot. (C) Cluster of mitotic associated proteins that are significantly regulated by LiCl in B. The functional network was determined using String 9.1 and color-coded based on the fold change in the microarray (Dataset S1). (D) Western blots of indicated proteins from Xenopus eggs (naturally arrested in metaphase II) and released into interphase with the Ca2+ ionophore A23187 for 25 min, treated with LiCl, or mock treated (NaCl). β-cat, β-catenin; cycE, cyclin E; Interph., interphase; M. II, metaphase II; pH3, phosphorylated histone 3. (E) Western blots of stage VI oocytes in Prophase I and Progesterone-matured (Prog.) oocytes in metaphase II. Oocytes were injected (Inj.) with Morpholinos (MO) or mRNA as indicated. Co, control; dnWnt11, dominant negative Wnt11; pH3, phosphorylated histone 3; PPL, preprolactin (negative control).
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    Image Search Results


    Gsk3 negatively regulates mitotic effectors in Xenopus extracts. (A) Scheme of the protein microarray experiment to assess Gsk3-dependent polyubiquitination. Interphase egg extracts were supplemented with ubiquitin, pretreated with LiCl or NaCl (Control), and then applied on protein arrays containing ∼9,000 proteins. Polyubiquitination of arrayed proteins (PolyUb) was monitored using anti-polyubiquitin antibodies and immunofluorescence detection using an array scanner. Signal intensities were transformed and are displayed as heat-map. (B) Distribution plot of polyubiquitination changes of 3,873 in vitro polyubiquitinated proteins after Gsk3 inhibition by LiCl (Log2[Control/LiCl]). Arrays were treated with 30 mM LiCl or 30 mM NaCl (Control). LiCl reduced polyubiquitination of 864 proteins >1.8-fold. Some candidates, associated with cell cycle progression and selected for further validation are indicated in the plot. (C) Cluster of mitotic associated proteins that are significantly regulated by LiCl in B. The functional network was determined using String 9.1 and color-coded based on the fold change in the microarray (Dataset S1). (D) Western blots of indicated proteins from Xenopus eggs (naturally arrested in metaphase II) and released into interphase with the Ca2+ ionophore A23187 for 25 min, treated with LiCl, or mock treated (NaCl). β-cat, β-catenin; cycE, cyclin E; Interph., interphase; M. II, metaphase II; pH3, phosphorylated histone 3. (E) Western blots of stage VI oocytes in Prophase I and Progesterone-matured (Prog.) oocytes in metaphase II. Oocytes were injected (Inj.) with Morpholinos (MO) or mRNA as indicated. Co, control; dnWnt11, dominant negative Wnt11; pH3, phosphorylated histone 3; PPL, preprolactin (negative control).

    Journal: Proceedings of the National Academy of Sciences of the United States of America

    Article Title: Maternal Wnt/STOP signaling promotes cell division during early Xenopus embryogenesis

    doi: 10.1073/pnas.1423533112

    Figure Lengend Snippet: Gsk3 negatively regulates mitotic effectors in Xenopus extracts. (A) Scheme of the protein microarray experiment to assess Gsk3-dependent polyubiquitination. Interphase egg extracts were supplemented with ubiquitin, pretreated with LiCl or NaCl (Control), and then applied on protein arrays containing ∼9,000 proteins. Polyubiquitination of arrayed proteins (PolyUb) was monitored using anti-polyubiquitin antibodies and immunofluorescence detection using an array scanner. Signal intensities were transformed and are displayed as heat-map. (B) Distribution plot of polyubiquitination changes of 3,873 in vitro polyubiquitinated proteins after Gsk3 inhibition by LiCl (Log2[Control/LiCl]). Arrays were treated with 30 mM LiCl or 30 mM NaCl (Control). LiCl reduced polyubiquitination of 864 proteins >1.8-fold. Some candidates, associated with cell cycle progression and selected for further validation are indicated in the plot. (C) Cluster of mitotic associated proteins that are significantly regulated by LiCl in B. The functional network was determined using String 9.1 and color-coded based on the fold change in the microarray (Dataset S1). (D) Western blots of indicated proteins from Xenopus eggs (naturally arrested in metaphase II) and released into interphase with the Ca2+ ionophore A23187 for 25 min, treated with LiCl, or mock treated (NaCl). β-cat, β-catenin; cycE, cyclin E; Interph., interphase; M. II, metaphase II; pH3, phosphorylated histone 3. (E) Western blots of stage VI oocytes in Prophase I and Progesterone-matured (Prog.) oocytes in metaphase II. Oocytes were injected (Inj.) with Morpholinos (MO) or mRNA as indicated. Co, control; dnWnt11, dominant negative Wnt11; pH3, phosphorylated histone 3; PPL, preprolactin (negative control).

    Article Snippet: Briefly, the arrays were washed in TBST and blocked for 4 h at 4 °C using Microarray Blocking solution (Arrayit), followed by a wash in lysis buffer.

    Techniques: Microarray, Ubiquitin Proteomics, Control, Immunofluorescence, Transformation Assay, In Vitro, Inhibition, Biomarker Discovery, Functional Assay, Western Blot, Injection, Dominant Negative Mutation, Negative Control