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sfk py527  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc sfk py527
    Sfk Py527, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 370 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+py527+src/Phospho-Src+(Tyr527)+Antibody/pm20583816__cb100099h_si_001-12-21-24
    Average 96 stars, based on 370 article reviews
    sfk py527 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Western Blot:

    Article Title: NAD + supplement potentiates tumor-killing function by rescuing defective TUB-mediated NAMPT transcription in tumor-infiltrated T cells.
    Article Snippet: Following incubation with the secondary antibody, membranes were washed with TBST for 5 mins at room temperature three times and then incubated with SuperSignal West Pico PLUS Chemiluminescent Substrate (Thermo Fisher) for visualization on film. .. The following antibodies were purchased from the indicated suppliers and used for immunoblotting (unless otherwise stated) at the indicated concentrations: anti-b-actin (Sigma, cat. no. A5441, clone AC-15); anti-NAMPT (Proteintech, cat. no. 66385-1-lg); Anti-Phosphotyrosine clone 4G10 (Millipore, cat. no. 05-321); antipY493 Zap70 (Cell signaling technology, cat. no. 2704); anti-Zap70 (Cell signaling technology, cat. no. 2705); anti-pZeta (Abcam, cat. no. ab68235); anti-Zeta (Abcam, cat. no. ab190728); anti-pErk (Cell signaling technology, cat. no. 9101); anti-Erk (Cell signaling technology, cat. no. 9102); anti-pY527 Src (Cell signaling technology, cat. no. 2105); anti-pY416 Src (Cell signaling technology, cat. no. 6943); anti-LCK (Cell signaling technology, cat. no. 2787; Biolegend, cat. no. LCK-01); anti-H3 (Cell signaling e6 Cell Reports 36, 109516, August 10, 2021 technology, cat. no.4499); anti-TUB (Proteintech, cat. no. 17928-1-AP); anti-GAPDH (Cell signaling technology, cat. no. 3683); anti-tubulin (Sigma cat. no. T6557). ..

    Membrane:

    Article Title: Effects of sex and DTNBP1 (dysbindin) null gene mutation on the developmental GluN2B-GluN2A switch in the mouse cortex and hippocampus
    Article Snippet: .. PSD enrichments (frontal cortex, 2 μg, or hippocampus, 4 μg) or membrane preparations (frontal cortex, 10 μg) were loaded on 7.5 % Tris-glycine polyacrylamide gels (Bio-Rad) and separated by electrophoresis at 200 V. Proteins were then transferred to Immobilon FL PVDF membranes (Millipore, Billerica, MA, USA) at 100 V for 1 h. They were cut at approximately 130 and 75 kDa (as indicated in Fig. and Additional file : Figure S2) and after blocking for 1 h in TBS blocking buffer (LI-COR Biosciences, Lincoln, NE, USA), were probed with the following primary antibodies overnight: anti-GluN1 (1:500; sc-1467, Santa Cruz Biotechnology, Dallas, TX, USA); anti-GluN2A (1:1000; sc-1468, Santa Cruz); anti-GluN2B (1:1000; 06-600, Millipore); anti-pY1472-GluN2B (1:500; #4208, Cell Signaling Technology, Danvers, MA, USA); anti-PSD-95 (1:5000; clone K28/43, UC Davis/NIH NeuroMab Facility); anti-SAP102 (1:2000; clone N19/2, UC Davis/NIH NeuroMab Facility); anti-PLCγ1 (1:250; sc-81, Santa Cruz); anti-Fyn (1:500; sc-16, Santa Cruz); anti-cSrc (1:1000; L4A1-2110S, Cell Signaling); anti-pY527-Src (1:500; #2105, Cell Signaling); and anti-dysbindin (1:1000, ab133652, Abcam, Cambridge, UK). .. Blots were then washed three times for 10 min in Tris-buffered saline containing 0.05 % Tween 20 (TBST) and probed for 1 h with secondary antibodies from LI-COR Biosciences: IRDye 800CW donkey anti-goat (926-32214); IRDye 680LT donkey anti-rabbit (926-68023); IRDye 800CW donkey anti-rabbit (926-32213); IRDye 680RD donkey anti-mouse (926-68072); and IRDye 680LT goat anti-mouse IgG1 specific (926-68050).

    Electrophoresis:

    Article Title: Effects of sex and DTNBP1 (dysbindin) null gene mutation on the developmental GluN2B-GluN2A switch in the mouse cortex and hippocampus
    Article Snippet: .. PSD enrichments (frontal cortex, 2 μg, or hippocampus, 4 μg) or membrane preparations (frontal cortex, 10 μg) were loaded on 7.5 % Tris-glycine polyacrylamide gels (Bio-Rad) and separated by electrophoresis at 200 V. Proteins were then transferred to Immobilon FL PVDF membranes (Millipore, Billerica, MA, USA) at 100 V for 1 h. They were cut at approximately 130 and 75 kDa (as indicated in Fig. and Additional file : Figure S2) and after blocking for 1 h in TBS blocking buffer (LI-COR Biosciences, Lincoln, NE, USA), were probed with the following primary antibodies overnight: anti-GluN1 (1:500; sc-1467, Santa Cruz Biotechnology, Dallas, TX, USA); anti-GluN2A (1:1000; sc-1468, Santa Cruz); anti-GluN2B (1:1000; 06-600, Millipore); anti-pY1472-GluN2B (1:500; #4208, Cell Signaling Technology, Danvers, MA, USA); anti-PSD-95 (1:5000; clone K28/43, UC Davis/NIH NeuroMab Facility); anti-SAP102 (1:2000; clone N19/2, UC Davis/NIH NeuroMab Facility); anti-PLCγ1 (1:250; sc-81, Santa Cruz); anti-Fyn (1:500; sc-16, Santa Cruz); anti-cSrc (1:1000; L4A1-2110S, Cell Signaling); anti-pY527-Src (1:500; #2105, Cell Signaling); and anti-dysbindin (1:1000, ab133652, Abcam, Cambridge, UK). .. Blots were then washed three times for 10 min in Tris-buffered saline containing 0.05 % Tween 20 (TBST) and probed for 1 h with secondary antibodies from LI-COR Biosciences: IRDye 800CW donkey anti-goat (926-32214); IRDye 680LT donkey anti-rabbit (926-68023); IRDye 800CW donkey anti-rabbit (926-32213); IRDye 680RD donkey anti-mouse (926-68072); and IRDye 680LT goat anti-mouse IgG1 specific (926-68050).

    Blocking Assay:

    Article Title: Effects of sex and DTNBP1 (dysbindin) null gene mutation on the developmental GluN2B-GluN2A switch in the mouse cortex and hippocampus
    Article Snippet: .. PSD enrichments (frontal cortex, 2 μg, or hippocampus, 4 μg) or membrane preparations (frontal cortex, 10 μg) were loaded on 7.5 % Tris-glycine polyacrylamide gels (Bio-Rad) and separated by electrophoresis at 200 V. Proteins were then transferred to Immobilon FL PVDF membranes (Millipore, Billerica, MA, USA) at 100 V for 1 h. They were cut at approximately 130 and 75 kDa (as indicated in Fig. and Additional file : Figure S2) and after blocking for 1 h in TBS blocking buffer (LI-COR Biosciences, Lincoln, NE, USA), were probed with the following primary antibodies overnight: anti-GluN1 (1:500; sc-1467, Santa Cruz Biotechnology, Dallas, TX, USA); anti-GluN2A (1:1000; sc-1468, Santa Cruz); anti-GluN2B (1:1000; 06-600, Millipore); anti-pY1472-GluN2B (1:500; #4208, Cell Signaling Technology, Danvers, MA, USA); anti-PSD-95 (1:5000; clone K28/43, UC Davis/NIH NeuroMab Facility); anti-SAP102 (1:2000; clone N19/2, UC Davis/NIH NeuroMab Facility); anti-PLCγ1 (1:250; sc-81, Santa Cruz); anti-Fyn (1:500; sc-16, Santa Cruz); anti-cSrc (1:1000; L4A1-2110S, Cell Signaling); anti-pY527-Src (1:500; #2105, Cell Signaling); and anti-dysbindin (1:1000, ab133652, Abcam, Cambridge, UK). .. Blots were then washed three times for 10 min in Tris-buffered saline containing 0.05 % Tween 20 (TBST) and probed for 1 h with secondary antibodies from LI-COR Biosciences: IRDye 800CW donkey anti-goat (926-32214); IRDye 680LT donkey anti-rabbit (926-68023); IRDye 800CW donkey anti-rabbit (926-32213); IRDye 680RD donkey anti-mouse (926-68072); and IRDye 680LT goat anti-mouse IgG1 specific (926-68050).



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