MIP1 | Aquaporin, glycerol transport activity

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AS15 2826   | clonality: polyclonal  |  host: rabbit  |  reactivity: Chlamydomonas reinhardtii 


30 st
Item No:
AS15 2826

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product information
Background MIP1 (Aquaporin, glycerol transport activity) is localized to the contractile vacuole, which in most freshwater flagellates is used to expel excess water.
Immunogen KLH-conjugated synthetic peptide, derived from Chlamydomonas reinhardtii MIP1, UniProt: Q5VLJ9
Host Rabbit
Clonality Polyclonal
Purity Affinity purified serum
Format Lyophilized in PBS pH 7.4
Quantity 50 ĩg
Reconstitution For reconstitution add 50 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 western blot (WB), immunogold (IG)
Related products

Chlamydomonas reinhardtii antibody collection

Algal protein extraction buffer

Secondary antibodies

Additional information to be added when available
application information
Recommended dilution

1 : 10 000 with ECL (WB), 1: 200 (IG)

Expected | apparent MW

31.5 | 43 kDa

Confirmed reactivity

Chlamydomonas reinhardtii (strains CC3395, and UVM4 from Neupert et al., 2009. (Generation of Chlamydomonas Strains that Efficiently Express Nuclear Transgenes.)

Predicted reactivity Chlamydomonas reinhardtii
Not reactive in

no confirmed exceptions from predicted reactivity are currently known

Additional information

As MIP1 is a membrane protein please use a high redox potential in your lysis buffer.

Selected references Komsic-Buchmann et al. (2014). The Contractile Vacuole as a Key Regulator of Cellular Water Flow in Chlamydomonas reinhardtii. Eukaryotic cell (13), Issue 11: 1421-30.

application example

western blot using anti-CreMIP1 antibodies
10 µg of total protein from 15ml cell suspension of Chlamydomonas reinhardtii CC3395, with a cell density of (~ 10 times 8) extracted with SDS buffer supplememnted with Protease inhibitor (cOmplete Ultra tablets, EDTA free, Roche, Mannheim), after removal of the cell debris via centrifugation, DTT was added (100mM final concentration) and were separated on 12 % SDS-PAGE and blotted 1h to PVDF using tank transfer. Blots were blocked with RotiBlock-Solution (Roth, Darmstadt) for 1h at room temperature (RT) or at 4°C ON with agitation. Blot was incubated in the primary antibody at a dilution of 1: 10,000 in TBS with 2% milk powder for 1h at RT with agitation. The antibody solution was decanted and the blot was washed 3 times for 10 minutes each with TBS-T at RT with agitation. Blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Sigma, St.Luis, MO) diluted to 1:80 000 in TBS tith 5% milk powder for 1h at RT with agitation. The blot was washed as above and developed for 1-2 min with ECL according to the manufacturer's instructions. Exposure time was 40 seconds.

Courtesy of Dr. Karin Komsic-Buchmann and Prof. Dr. Burkhard Becker, University of Cologne, Germany

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