SE | Serrate RNA effector molecule (chicken antibody)

AS15 2836 | Clonality: Polyclonal | Host: Chicken | Reactivity: Arabidopsis thaliana

SE | Serrate RNA effector molecule (chicken antibody) in the group Plant/Algal Antibodies / DNA/RNA/Cell Cycle / microRNA at Agrisera AB (Antibodies for research) (AS15 2836)


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product information

Serrate RNA effector molecule is required for proper processing of primary miRNAs to miRNA. Also critical for the accumulation of the trans-acting small interfering RNA (ta-siRNA).


KLH-conjugated synthetic peptide chosen from Arabidopsis thaliana serrate protein sequence Q9ZVD0, At2g27100

Host Chicken
Clonality Polyclonal
Purity Affinity purified serum in PBS, pH 7.4
Format Liquid in PBS pH 7.4 with 0.02 % sodium azide
Quantity 50 ĩg
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)
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AS09 532 | anti-Serrate RNA effector molecule, rabbit antibodies

collection of antibodies to micro RNA

Plant protein extraction buffer

Secondary antibodies

Additional information
application information
Recommended dilution 1 : 2000 (WB)
Expected | apparent MW

81 | 80 kDa

Confirmed reactivity Arabidopsis thaliana
Predicted reactivity Nicotiana benthamina, Nicotiana tabacum, Saccharum hybrid cultivar NCo 376, Zea mays
Not reactive in No confirmed exceptions from predicted reactivity are currently known.
Additional information Over night incubation with anti-serrate antibodies is not recommended as it can contribute to increased background signal. 
Selected references to be added when available, antibody released in February 2016.

application example

western blot using chicken anti-serrate antibodies

30 µg of total protein from 14-day-old seeldlings of Arabidopsis thaliana was extracted with extraction buffer containing: 100 mM Tris HCl, 10 % glycerol, 5 mM EGTA, 0.15 M NaCl, 0.75 % Triton X100, 0.05 % SDS, 1mM DTT, 1x Complete Mini EDTA-free protease inhibitor (Roche) were separated on 10 % SDS/PAGE using semi-dry transfer and blotted 1 h to PVDF. Blots were blocked with 5 % milk in TBS+0.1 % Tween for 1 h at RT with agitation. Blot was incubated in the primary antibody at a dilution of 1: 2000 in TBS-T for 1 h at RT with agitation. Blot was incubated in secondary antibody (goat anti-chicken HRP conjugated, AS10 1489 Agrisera) in 1: 10 000 diution for 1 h at RT with agitation in TBS 0.2 % Tween. The blot was washed as above and developed for 5 minutes with ECL Prime, GE Healthcare, according to manufacturer's instructions. Exposure time was 10 min.

Courtesy of M.Sc. Agata Stępień, Department of Gene Expression, Adam Mickiewicz University, Poland

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