40818 DATASHEET PDF

3. Ordering information. 4. Functional diagram. HEFB. Quad 2-input AND gate. Rev. 8 — 15 December Product data sheet. Table 1. Ordering. Details, datasheet, quote on part number: ZL Application Notes) Ordering Information ZL/DCE ZL/DCF (tubes) 8 pin SOIC (tape and reel) 8. Cat. No. / Cat. No. / System (w/micro CA). Cat. No. Cat. No. / Cat. No. / Removable Drum Only.

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Solutions and Reagents Achieve higher quality immunofluorescent images using the efficient and cost-effective, pre-made reagents in our Immunofluorescence Application Solutions Kit NOTE: Carefully remove the buffer once the solution is clear. Repeat washing step once more. Transfer supernatant containing phosphorylated substrate to another tube. Microcentrifuge for 5 min. Volumes are for 10 cm x 10 cm cm 2 of membrane; for different sized membranes, adjust volumes accordingly.

This protocol is intended for immunoprecipitation of native proteins for analysis by western daatsheet or kinase activity utilizing Protein A magnetic separation. Pre-wash magnetic beads just prior to use: Primary Antibody Dilution Buffer: Dxtasheet higher quality immunofluorescent images datassheet the efficient and cost-effective, pre-made reagents in our Immunofluorescence Application Solutions Kit. Incubate for at least 5 min at room temperature.

More about how we get our images. Wash three times for 5 min each with 15 ml of TBST.

Prepare solutions with reverse osmosis deionized RODI or equivalent grade water. Keep on ice between washes. Vortex, then microcentrifuge for 30 datxsheet. Analyze cells in DNA staining solution on flow cytometer.

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Find answers on our FAQs page. Immunoprecipitation Cell Lysate Datashete Optional A cell lysate pre-clearing step is highly recommended to reduce non-specific protein binding to the Protein A Magnetic beads. Incubate specimen in fluorochrome-conjugated secondary antibody diluted in Antibody Dilution Buffer for 1—2 hr at room temperature in the dark.

While blocking, datsaheet primary antibody by diluting as indicated on datasheet in Antibody Dilution Buffer. Additionally, it is recommended that you verify the removal of the first antibody complex prior to reprobing so that signal attributed to binding of the new antibody is not leftover signal from the first immunoblotting experiment.

Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube.

ZL Datasheet pdf – GHz Fixed Modulus Divide 4 Prescaler – Zarlink Semiconductor

Would you like to visit your country specific website? Place the tube in a magnetic separation rack for seconds.

Separate the beads from the lysate using a magnetic separation rack, transfer the pre-cleared lysate to a clean tube, and discard the magnetic bead pellet.

Discard supernatant in appropriate waste container. Electrotransfer to nitrocellulose membrane Resuspend cells in 0.

Phospho-STING (Ser366) (D8K6H) Rabbit mAb #40818

The supernatant is the cell lysate. Ubiquitinating enzymes UBEs catalyze protein ubiquitination, a reversible process countered by deubiquitinating enzyme DUB action 1,2.

Treat cells by adding fresh media containing regulator for desired time. Fix for 15 min at room temperature.

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Application Dilutions Immunofluorescence Immunocytochemistry 1: Formaldehyde is toxic, use only in a fume hood. Aspirate fixative, rinse three times in 1X PBS for 5 min each. Dilute to 1X with dH 2 O. Western blot analysis of extracts from various cell lines using USP8 Antibody. Recommended Satasheet secondary antibodies: ATP 10 mM for kinase assays: A cell lysate pre-clearing step is highly dtaasheet to reduce non-specific protein binding to the Protein A Magnetic beads. From sample preparation to detection, the reagents you need dztasheet your Western Blot are now in one convenient kit: Analyze sample by western blot see Western Immunoblotting Protocol.

Detection of Proteins Directions for Use: Incubate with rotation for 20 minutes at room temperature. Sample Analysis Proceed to one of the following specific set of steps.

CST – Phospho-STING (Ser) (D8K6H) Rabbit mAb

Reprobing of an existing membrane is a convenient means to immunoblot for multiple proteins independently when only a limited amount of sample is available. Allow datasheef to fix for 15 min at room temperature.

Solutions and Reagents From sample preparation to detection, the reagents you need for your Western Blot are now in one convenient kit: