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51116 DATASHEET PDF

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Would you like to visit your country specific website? These results suggest that fragile X syndrome is related to abnormal translation caused by defects in RNAi-related pathways.

Aspirate media from cultures; wash cells with 1X PBS; aspirate. Wash three times for 5 min each with 15 ml of TBST.

Fragile X syndrome is a genetic disorder characterized by a spectrum datasheeh physical and behavioral features and is a frequent form of inherited mental retardation 1. Volumes are for 10 cm x 10 cm cm 2 of membrane; for different sized dqtasheet, adjust volumes accordingly.

Find answers on our FAQs page. Protein Blotting A general protocol for sample preparation. Reprobing can be a valuable method but with each reprobing of a blot there is potential for increased background signal.

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Solutions and Reagents From sample preparation to detection, the reagents you need for your Western Blot are now in datashee convenient kit: Application Dilutions Western Blotting 1: Detection of Proteins Directions for Use: Immediately scrape the cells off the plate and transfer the extract to a microcentrifuge tube.

Proceed with detection Section D. Blotting Membrane and Paper: Electrotransfer to nitrocellulose membrane Each of the fragile X proteins can self-associate, as well as form heteromers with the other two related proteins 3. Reprobing of an existing membrane is a convenient means to immunoblot for multiple proteins independently when only a limited amount of sample is available. From sample preparation to detection, the reagents you need for your Western Blot are now in one convenient kit: Dataaheet cells by adding fresh media containing regulator for desired time.

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Biotinylated Protein Ladder Detection Pack: This can be done by re-exposing the blot to ECL reagents and making sure there is no signal prior to adding the next primary antibody. Do not aliquot the antibody.

Prepare solutions datasheeet reverse osmosis deionized RODI or equivalently purified water. Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to the sequence of human FXR2 protein.

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FXR2 Antibody – Incubate membrane in 25 ml of blocking buffer for 1 hr at room temperature. Sonicate for 10—15 sec to complete cell lysis and shear DNA to reduce sample viscosity. Please refer to primary antibody datasheet or product webpage for recommended antibody dilution.

Primary Antibody Dilution Buffer: Incubate substrate with membrane for 1 minute, remove excess solution membrane remains wetwrap in plastic and expose to X-ray film.

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. Microcentrifuge for 5 min.

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To Purchase S View datwsheet. Dilute to 1X with dH 2 O. Changing to another country might result in loss of shopping cart. Antibodies are purified by protein A and peptide affinity chromatography.