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AS15 3095 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Arabidopsis thaliana


5 st
Item No:
AS15 3095

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product information

HEN1 (HUA ENHANCER 1) is a methyltransferase that can methylate 3'-end of miRNAs, siRNas and trans-acting small interfering RNAs (ta-siRNAs). This protein protects the 3'-end of sRNAs from uridylation activity and degradation by adding a methyl group to the ribose of the last nucleotide of sRNAs.

Alternative protein names: Small RNA 2'-O-methyltransferase, Protein CORYMBOSA 2, S-adenosylmethionine-dependent RNA methyltransferase HEN1.

Immunogen KLH-conjugated peptide derived from Arabidopsis thaliana HEN1 sequence, Uniprot: Q9C5Q8, TAIR: AT4G20910
Host Rabbit
Clonality Polyclonal
Purity Affinity purified serum
Quantity 200 ĩg
Reconstitution For reconstitution add 200 ĩl of sterile water.

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
Related products

collection of antibodies to proteins involved in microRNA metabolism

collection of antibodies to proteins involved in plant development

Plant protein extraction buffer

Secondary antibodies

Additional information
application information
Recommended dilution 1: 1000 - 1: 5000 for ECL (WB)
Expected | apparent MW

104.5 kDa | 105 kDa

Confirmed reactivity

Arabidopsis thaliana

Predicted reactivity please inquire
Not reactive in

no confirmed exceptions from predicted reactivity are currently known

Additional information

to be added when available

Selected references

to be added when available, antibody released in January 2016.

application example

western blot using anti-HEN1 antibodies

50 µg of total protein from Arabidopsis thaliana whole vegetative rosette wild type Col-0 (a) and HEN1 overexpression mutant (b) extracted with extraction buffer (50 mM Tris pH 7.5; 150 mM NaCl; 1 mM EDTA; 10 % v/v Glycerin; 1 mM DTT, 1x Complete Protease Inhibitor Cocktail, Roche) and denatured with Laemmli buffer at 95°C/5 min., were separated on 7.5 % SDS-PAGE and blotted 1.5 h to PVDF using tank transfer. Blots were blocked with blocking buffer (5% milk powder; 1x TBS; 0.1% Tween-20) overnight at 4°C with agitation. Blot was incubated in the primary antibody at a dilution of 1:1000 for 2h at RT with agitation. The antibody solution was decanted and the blot was rinsed briefly and then washed tree times for 15 min in TBS-T at RT with agitation. Blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Agrisera, AS09 602) diluted to 1:20 000 in blocking buffer for 1h at RT with agitation. The blot was washed as above and developed for 5 min with Amersham ECL Prime and expose to Amersham Hyperfilms ECL for 20 seconds.

Courtesy of Dr. Pablo Manavella, Instituto de Agrobiotecnología del Litoral (IAL), Argentina

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