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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Rinse three times in 1X PBS for 5 min each. Pre-wash magnetic beads just prior to use: Solutions and Reagents Achieve higher quality immunofluorescent images using the efficient and cost-effective, pre-made reagents in our Immunofluorescence Application Solutions Kit NOTE: Reprobing can be a valuable method but with each reprobing of a blot there is potential for increased background signal.

USP8 Antibody – Proceed with Immunostaining Section C. Treat cells by adding fresh media containing regulator for desired time. Briefly vortex the stock tube to resuspend the magnetic beads. Formaldehyde is toxic, use only in a fume hood. Analyze cells in DNA staining solution on flow cytometer. Repeat washing step once more.


Ubiquitinating enzymes UBEs catalyze protein ubiquitination, a reversible process countered by deubiquitinating enzyme DUB action 1,2. Incubate 30 min on ice.

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

Collect cells by centrifugation and aspirate supernatant. Recommended Fluorochrome-conjugated Dqtasheet secondary antibodies: Proceed to analyze by western immunoblotting or kinase activity section D. Wash cells by centrifugation in excess 1X PBS to remove methanol. Protein A Magnetic Beads: Western blot analysis of extracts from various cell lines using USP8 Antibody. Mizuno E et al. Research studies have shown that USP8 is an essential growth-regulated enzyme indespensible for cell proliferation and survival 3,4.

Vortex, then microcentrifuge for fatasheet sec. The optimal lysate concentration will depend on the expression level of the protein of interest. Transfer the supernatant to a new tube.

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

Incubate substrate with membrane for 1 minute, remove excess solution membrane remains wetwrap in plastic and expose to X-ray film. Biotinylated Protein Ladder Detection Pack: Please refer to primary antibody datasheet or product webpage for recommended antibody dilution. Aspirate fixative, rinse three times in 1X 408118 for 5 min each. Pre-wash magnetic beads just prior to use:.


Antibodies are purified by protein A and peptide affinity chromatography. Analyze sample by western blot see Western Immunoblotting Protocol.

Allow cells to fix for 15 min at room temperature. Wash three times for 5 min each with 15 ml of TBST.

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

Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ser of human STING protein. 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. dayasheet

The supernatant is the sample. Do not aliquot the antibody.