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GST1 | Glutathione-S-transferase

265 €
Buy 2 items of this product for 198 €/each
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AS15 2883 | clonality: polyclonal | host: rabbit | reactivity: Chlamydomonas reinhardtii

PRODUCT INFORMATION IN PDF

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AS15 2883

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product information
Background Glutathione-S-transferase (GST1) is an enzyme which belongs to GST superfamily and has a transferase activity.
Immunogen

KLH-conjugated synthetic peptide derived from Glutathione-S-transferase protein sequence from Chlamydomonas reinhardtii, UniProt: A8JBA7

Host Rabbit
Clonality Polyclonal
Clone
Purity Affinity purified serum
Format Lyophilized in PBS pH 7.4
Quantity 50 ĩg
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 AS15 2882 | anti-GPXh | Glutathione peroxidase, rabbit antibodies
Collection of antibodies to Chlamydomonas reinhardtii proteins
Additional information
application information
Recommended dilution

1: 5000 ECL (WB)

Expected | apparent MW

23.9 kDa

Confirmed reactivity Chlamydomonas reinhardtii
Predicted reactivity Volvox carteri
Not reactive in
Additional information
Selected references to be added when available, antibody released in July 2015

application example

western blot using anti-algal GST1 antibodies

10 µg of total protein from Chlamydomonas reinhardtii extracted with 2 % SDS/50 mM TRIS pH 6.8 + protease inhibitor cocktail were separated on 12 % SDS-PAGE and blotted for 1 h to PVDF using semi-dry transfer. Blots were blocked with 5 % low-fat milk powder TBS + 0.1 % Tween for 1h at room temperature (RT) with agitation. Blot was incubated in the primary antibody at a dilution of 1: 5 000 for 1 h at RT with agitation. The antibody solution was decanted and the blot was rinsed, then washed 3 times each for 5 min in TBS-T at RT with agitation. Blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated) diluted to 1:25 000 in 2 % low-fat milk powder TBS + 0.1 % Tween for 1h at RT with agitation. The blot was washed as above and developed for 30 s with ECL (Amersham) according to the manufacturer's instructions. Exposure time was typically 30 seconds.

Courtesy Dr. Thomas Roach, University of Innsbruck, Austria

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