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N-YFP | N-terminal of YFP

265 €
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AS11 1776 | Clonality: polyclonal | Host: rabbit | Reactivity:N-terminal of YFP

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AS11 1776

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product information
Background YFP (Yellow Fluorescent Protein) is a genetic mutant of green fluorescent protein (GFP). YFP has an excitation peak at 514 nm and emission peak at 527 nm.
Immunogen

KLH-conjugated synthetic peptide derived from N-terminal of YFP protein.

Host Rabbit
Clonality Polyclonal
Clone
Purity Serum
Format Lyophilized
Quantity 50 µl
Reconstitution

For reconstitution add 50 ĩl of sterile water.

Storage

Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.

Tested applications Western Blot (WB)
Related products

AS11 1775 | anti-C-YFP | C-terminal of YFP, rabbit antibodies

Collection of antibodies to fluorsecent tags
Collection of antibodies to tag proteins

Plant and algal protein extraction buffer

Secondary antibodies

Additional information
application information
Recommended dilution

1 : 2000 (WB)

Expected | apparent MW
Confirmed reactivity N-YFP tagged proteins from Arabidopsis thaliana, E.coli, Nicotiana tabacum
Predicted reactivity
Not reactive in

no confirmed exceptions from predicted reactivity are currently known

Additional information YFP molecular weight is 27 kDa, however detected band is going to have MW increased by a fused protein. 
Selected references

To be added when available, antibody released in May 2016.


Application example

western blot using anti-N-YFP polyclonal antibodies

Sample preparation and immunoblot analysis were carried out as described in Karnik et al., Plant Cell 2015, March 2015 vol. 27 no. 3 675-694. For immunoblot analysis of plant tissues,leaves were excised and flash frozen in liquid N2. Frozen tissue was ground in equal volumes (w/v) of homogenization buffer containing 500 mM sucrose, 10% glycerol, 20 mM EDTA,20mMEGTA,ProteaseInhibitor(Roche),10mMascorbicacid,5mM DTT, and 50 mM Tris-HCl, pH 7.4, and centrifuged at 13,000g and 4°C for 30 min to pellet debris. Supernatant was diluted 1:1 in 23 Laemmli buffer containing 2.5% 2-mercaptoethanol, heated to 95°C for 10 min, and separated by SDS-PAGE on a 12% Acrylamide gel. Ponceau S-stained Rubisco bands were used as loading standards for plant samples. Membrane type: Cellulose Nitrate (GE Healthcare) Blocking reagent: GE Healthcare Wash buffer: Tris Buffered Saline, 0.5% Tween Exposure time: 10 – 20 seconds.

Courtesy of Dr. Rucha Karnik, University of Glasgow, UK


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