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Anti syntaxin 1a

Manufactured by Merck Group

Anti-syntaxin 1A is a laboratory reagent used for the detection and quantification of syntaxin 1A, a membrane-associated protein involved in synaptic vesicle docking and fusion. It can be used in various immunoassay techniques to analyze the expression and localization of syntaxin 1A in biological samples.

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2 protocols using anti syntaxin 1a

1

Calcium Channel Protein Expression

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Primary antibodies used included anti-Cav2.1 (1:500, Alomone Labs), anti-GFP rabbit polyclonal (1:2000, Invitrogen/Thermo Fisher Scientific), anti-GAPDH (1:3000, Novus Biologicals), anti-transferrin receptor (1:1000, Invitrogen/Thermo Scientific), anti-CACNA2D1 (1:1000, Abcam), anti-Cavβ4 (1:1000, Neuromab), anti-AnkB (1:500, Thermo Fisher Scientific), and anti-syntaxin 1A (1:5000, Millipore Sigma). Secondary antibodies used included horseradish peroxidase (HRP)-conjugated AffiniPure donkey anti-rabbit immunoglobulin and donkey anti-mouse IgG (all at 1:4000; Jackson ImmunoResearch).
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2

Protein Expression Analysis in Neurons

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Mouse antibody anti-syntaxin 1A (1:5000; S0664; HPC-1) and rabbit antibody anti-APP (1:3000; A8717) were obtained from MilliporeSigma (Burlington, MA); rabbit antibody anti-SNAP25 (1:2000; 14903-1-AP), anti-NPTX2 (10889-1-AP), mouse antibodies anti-synaptophysin (1:5000; 67864-1-Ig), anti-β-actin (1:10,000; 60008-1-Ig) were from Proteintech (Rosemont, IL). Mouse antibody anti-synaptobrevin 2 (1:5000; 104 211), rabbit anti-neurofilament L (171 002), and anti-syntaxin 1B (110 402) were purchased Synaptic Systems (Goettingen, Germany). Mouse antibody anti-synaptotagmin (1:2000; 610434) was from BD Biosciences (Franklin Lakes, NJ). Rabbit antibodies anti-synapsin 1 (1:5000; 5297) and anti-synaptojanin 1 (1:1000; 80377) were got from Cell Signaling Technology (Danvers, MA). Mouse antibody anti-SV2A (1:5000; sc-376234) was obtained from Santa Cruz Biotechnology (Dallas, TX). Mouse antibody anti-PSD95 (1:2000; 7E3-1B8) was from ThermoFisher Scientific (Waltham, MA). In all cases, a single band or in some cases doublet, at the expected molecular weight was quantitated. Bands at other molecular weights, of uncertain identify, were detected with some antibodies; they were usually of lesser intensity and were not included in our analysis.
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