S TRANSISTOR (PNP). FEATURE. Excellent hFE linearity. MAXIMUM RATINGS (TA=25℃ unless otherwise noted). Symbol. Parameter. Value. Units. Order Number Normal Lead Free Plating S-x-TK SL-x-TK Package SOT TO Pin Details, datasheet, quote on part number: S. Part, S-TO Category. Description, LOW Voltage HIGH Current Small Signal PNP Transistor. Company, Unisonic Technologies. Datasheet, Download .
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Proceed to analyze by western immunoblotting or kinase activity section D. Keep on ice between washes.
Sonicate for 10—15 sec to complete cell lysis and shear DNA to reduce sample viscosity. Solutions and Reagents From sample preparation to detection, the reagents you need for your Western Blot are now in one convenient kit: Scrape cells off the plate and transfer to microcentrifuge tubes.
Prepare solutions with reverse osmosis deionized RODI or equivalently purified water.
Sample Analysis Proceed to one of the following specific set of steps. Immunoprecipitation for Native Proteins This protocol is intended for immunoprecipitation of native proteins for analysis by western immunoblot or kinase activity utilizing Protein A magnetic separation. To harvest cells under nondenaturing conditions, remove media and rinse cells once with ice-cold 1X PBS. It should be noted that for the best possible results a fresh blot is always recommended.
The supernatant is the cell lysate. Application Dilutions Western Blotting 1: Prepare solutions with reverse osmosis deionized RODI or equivalent grade water. Protein Blotting A general protocol for sample preparation.
S Datasheet, Equivalent, Cross Reference Search. Transistor Catalog
From sample preparation to detection, the reagents you need for your Western Blot are now in one convenient datasheft ATP 10 mM for kinase assays: Remove PBS and add 0. Wash three times for 5 min each with 15 ml of TBST.
Dilute to 1X with dH 2 O. Pre-clear enough lysate for test samples and isotype controls.
Protein A Magnetic Beads: The supernatant is the sample. To Purchase S View sizes.
Would you like to datasneet your country specific website? A cell lysate pre-clearing step is highly recommended to reduce non-specific protein binding to the Protein A Magnetic beads. Pre-wash magnetic beads just prior to use: Pre-wash magnetic beads see Cell Lysate Pre-Clearing section, steps 1 and 2. Electrotransfer to nitrocellulose membrane Carefully remove the buffer once the solution is clear.
Please refer to primary antibody datasheet or product webpage for recommended antibody dilution.
PNP SILICON TRANSISTOR
Pellet beads using magnetic separation rack. Preparing Cell Lysates Aspirate media. This protocol is intended for immunoprecipitation of native proteins for analysis by western immunoblot or kinase activity utilizing Protein A magnetic separation. Changing to another country might result in loss of shopping cart. The optimal lysate concentration will depend on the expression level of the protein of interest. Sonicate on ice three times for 5 sec each. Dataheet the tube in a magnetic separation rack for seconds.
Incubate with rotation for 20 minutes at room temperature. Detection of Proteins Directions for Use: MKK3 and MKK6 datashwet both activated by different forms of cellular stress and inflammatory cytokines 4,5. Do not aliquot the antibody. Repeat washing step once more. Aspirate media from cultures; wash cells with 1X PBS; aspirate.
Immunoprecipitation Cell Lysate Pre-Clearing Optional A cell lysate pre-clearing step is highly recommended to reduce non-specific protein binding to the Protein Datasheett Magnetic beads.
Remove buffer once solution is clear.