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> AGO1 | Argonaute 1, Blocking peptide

AGO1 | Argonaute 1, Blocking peptide

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Referencia AS09527P

embalaje : 100ug

Marca : Agrisera

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AGO1 | Argonaute 1, Blocking peptide

Product no: AS09 527P

AS09 527P |  Blocking peptide

    Product Info
    Format: Lyophilized
    Quantity: 100 µg
    Reconstitution: For reconstitution please add sterile water
    Storage: Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.
    Tested applications: Neutralization assay (NeA)
    Expected | apparent MW: 1716.9 Da
    Additional Information
    Additional information:

    Estimation of the ratio between antibodies and peptide : In neutralisation assay use 9.16 µg of argonaute 1 peptide for 10 ml of reaction volume.

    In case of any questions please contact [email protected]
    Additional information (application): Due to its low molecular weight, this peptide is not suitable for separation on a SDS gel,
    Background
    Background:

    This blocking peptide can be used as a control to neutralize AGO1 | argonaute 1 before immunolocalization or western blot. Furter details are provided below.

    AGO1     belongs to a group of argonaute proteins which are catalytic component of the RNA-incudes silencing complex (RISC). This protein complex is responsible for the gene silencing (RNAi).
    Protocols Peptide neutralization assay


    TCA/Acetone protein precipitation method for plant proteins


    • Grind plant tissue in a liquid nitrogen. Continue grinding with 10% TCA solution in acetone (ice cold).Precipitate overnight in -20C.Spin at 4°C for 1min, 17k rpm > wash with ice cold acetone until you obtain a white pellet.Dissolve the pellet in buffer of choice (for example 8M urea containing 5mM DTT, or denaturate in SDS protein loading buffer for 10 min. at 70°C)Clarify supernatantMeasure protein concentration. Proceed with a western blot.

    Example of a western blot result obtained with this method, which allows high protein load per well, can be found below. 



    360 µg/well of Arabidopsis thaliana protein extracted by TCA-acetone precipitation from floral tissue and saturated in 8M urea were separated on 15% SDS-PAGE and blotted for 1hour to 0.2 µm nitrocellulose at 100V using wet transfer system. Blots were blocked with 0.5% cold fish gelatin for 1hr at room temp with agitation. Blot was incubated in the primary antibody at a dilution of 1:2500 for an hour at RT with agitation. The blots were washed with 3X 15min TBS-TT at RT with agitation. Blots as incubated in the secondary antibody (DayLight 800) 1:5000 dilution for 30 min. at RT with agitation and washed 1X with TBSTT for 15 min, 1X with TBST for 15min before scanning with the ODyssey IRD scanner.

    Courtesy of Dr. Betty Chung and Pawel Baster, University of Cambridge, United Kingdom

    BACK to Plant Protocols page Reviews:
  • Katarzyna Niedojadło | 2013-02-27
    0 | 0
    I checked this antibodies by immunocytochemistry but I have many problems with Western blotting.