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Alexa fluor 680 conjugated anti mouse igg

Manufactured by Thermo Fisher Scientific

The Alexa Fluor 680 conjugated anti-mouse IgG is a fluorescently labeled secondary antibody used to detect and visualize mouse primary antibodies in various immunoassay techniques. The Alexa Fluor 680 dye provides a bright, photostable fluorescent signal.

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4 protocols using alexa fluor 680 conjugated anti mouse igg

1

Hippocampal Protein Extraction and Analysis

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Individual hippocampi were sonicated in lysis buffer (10mM Tris, pH7.4, 100 mM NaCl, 1 mM EDTA, 1mM EGTA, 1mM NaF, 20 mM Na 4 P 2 O 7, 2mM Na 3 VO 4, 1% Triton X-100, 10 % glycerol, 0.1% SDS, and 0.5% deoxycholate) with Complete protease inhibitor cocktail (Roche, Indianapolis, IN) as we have previously published (14 (link)). Reducing agent (Thermo Scientific, Waltham, MA) and LDS (Thermo) were added to each sample. 20–30 μg of total protein was separated using NuPAGE 4–12% Bis-Tris gels (Thermo) and transferred onto nitrocellulose membrane (Bio-Rad, Hercules, CA) as previously described (13 (link)). Using Rockland (Pottstown, PA) Blocking Buffer for Fluorescent Western Blotting and the following antibodies, the blots were imaged and analyzed with Odyssey infrared scanning (LiCor Bioscience, Lincoln, NE) as previously described. Mouse monoclonal anti-β-actin antibody was purchased from Sigma-Aldrich (St. Louis, MO) and used at 1:10,000. Primary antibodies purchased from Cell Signaling Technology (Danvers, MA) and used at 1:500 included: pS6K (Thr389, #9205), S6K (#9202), pAkt (Ser473, #9271), pAkt (Thr308, #9275), Akt (#9272), p-mTOR (Ser2448, #2971), mTOR (#2972), pAMPKα (Thr172, #2531), AMPKα (#2532). Secondary antibodies were Alexa Fluor 680 conjugated anti-mouse IgG (1:12,500, Thermo) and Infrared Dye 800 conjugated anti-rabbit IgG (1:12,500, Rockland).
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2

Hippocampal Protein Extraction and Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Individual hippocampi were sonicated in lysis buffer (10mM Tris, pH7.4, 100 mM NaCl, 1 mM EDTA, 1mM EGTA, 1mM NaF, 20 mM Na 4 P 2 O 7, 2mM Na 3 VO 4, 1% Triton X-100, 10 % glycerol, 0.1% SDS, and 0.5% deoxycholate) with Complete protease inhibitor cocktail (Roche, Indianapolis, IN) as we have previously published (14 (link)). Reducing agent (Thermo Scientific, Waltham, MA) and LDS (Thermo) were added to each sample. 20–30 μg of total protein was separated using NuPAGE 4–12% Bis-Tris gels (Thermo) and transferred onto nitrocellulose membrane (Bio-Rad, Hercules, CA) as previously described (13 (link)). Using Rockland (Pottstown, PA) Blocking Buffer for Fluorescent Western Blotting and the following antibodies, the blots were imaged and analyzed with Odyssey infrared scanning (LiCor Bioscience, Lincoln, NE) as previously described. Mouse monoclonal anti-β-actin antibody was purchased from Sigma-Aldrich (St. Louis, MO) and used at 1:10,000. Primary antibodies purchased from Cell Signaling Technology (Danvers, MA) and used at 1:500 included: pS6K (Thr389, #9205), S6K (#9202), pAkt (Ser473, #9271), pAkt (Thr308, #9275), Akt (#9272), p-mTOR (Ser2448, #2971), mTOR (#2972), pAMPKα (Thr172, #2531), AMPKα (#2532). Secondary antibodies were Alexa Fluor 680 conjugated anti-mouse IgG (1:12,500, Thermo) and Infrared Dye 800 conjugated anti-rabbit IgG (1:12,500, Rockland).
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3

Western Blot Analysis of Oxidative Stress Markers

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Dopamine hydrochloride, 3–4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA) were all purchased from Sigma (St Louis, MO). Halt protease and phosphatase inhibitor cocktail was obtained from Thermo Fisher (Waltham, MA). Bradford assay reagent and Western blotting buffers were purchased from Bio-Rad (Hercules, CA). Anti-4-hydroxynonenal antibody was purchased from R&D Systems (MAB3249, Minneapolis, MN (Ghosh et al., 2016 (link))), while anti-BDNF was purchased from Santa Cruz Biotechnology (sc-546, Dallas, TX). CREB and p-CREB (Ser133) antibodies were obtained from Cell signaling (9104, 87G3, Boston, MA (Jin et al., 2011 (link))). The anti-mouse and anti-rabbit secondary antibodies (Alexa Fluor 680 conjugated anti-mouse IgG and IRdye 800 conjugated anti-rabbit IgG) were purchased from Invitrogen and Rockland Inc., respectively.
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4

Neurochemical and Antibody Analysis Protocol

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Dopamine hydrochloride, 3-4-dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), 3,3′-diaminobenzidine (DAB), manganese chloride (MnCl2), and hydrogen peroxide were all purchased from Sigma (St Louis, MO). Halt protease and phosphatase inhibitor cocktail was obtained from Thermo Fisher (Waltham, MA). Bradford assay reagent and Western blotting buffers were purchased from Bio-Rad Laboratories (Hercules, CA). Anti-4-hydoxynonenal (4-HNE) antibody was purchased from R&D Systems (Minneapolis, MN). We purchased anti-IBA-1 antibodies from Wako Pure Chemical Industries (Richmond, VA) and Abcam (Cambridge, MA) for immunohistochemistry (IHC) and Western blot, respectively. Anti-tyrosine hydroxylase (TH) antibody was purchased from Millipore (Billerica, MA). Anti-oligomeric antibody (A11) and cell culture reagents were purchased from Invitrogen. The anti-mouse and anti-rabbit secondary antibodies (Alexa Fluor 680 conjugated anti-mouse IgG and IRDye 800 conjugated anti-rabbit IgG) were purchased from Invitrogen and Rockland Inc., respectively.
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