PsaH | PSI-H subunit of photosystem I, Chlamydomonas

345 €

AS06 143  |  clonality: polyclonal  |  host: rabbit  |  reactivity: Chlamydomonas reinhardtii


51 st
Item No:
AS06 143

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product information

PsaH (PSI-H) is a conserved subunit of type I photosynthetic reaction centers (Photosystem I, PSI). PSI is an integral membrane multi-protein complex that catalyzes the electron transfer from plastocyanin (or cytochrome c6) to ferredoxin (or flavodoxin). Psa-H has been suggested to be involved in regulation of state1-state2 transitions. In plants and green algae Psa-H is nuclear encoded and imported post-translationally into the chloroplast where it inserts into the thylakoid membrane.


Recombinant PsaH protein from Chlamydomonas reinhardtii P13352

Host Rabbit
Clonality Polyclonal
Purity Serum
Format Lyophilized
Quantity 200 ĩl
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 western blot (WB)
Related products

AS06 105 PsaH | PSI-H subunit of photosystem I

PSI available antibodies to Photosystem I proteins

Photosynthesis available antibodies to photosynthetic proteins

Collection of antibodies to Chlamydomonas proteins

Plant protein extraction buffer

Secondary antibodies

Additional information
application information
Recommended dilution

1:10 000 from with standard ECL (WB)

Expected | apparent MW

10 | 10 for Chlamydomonas reinhardtii

Confirmed reactivity

Arabidopsis thaliana (weak), Chlamydomonas reinhardtii, Hordeum vulgare

Predicted reactivity

Chlamydomonas reinhardtii

Not reactive in

Synechococcus sp. PCC 7942

Additional information

to be added when available

Selected references

Winck (2011). Nuclear proteomics and transcription factor profiling. Dissertation, University of Posdam.

application example

2 µg of total leaf protein of Arabidopsis thaliana (1) and Hordeum vulgare (2) and total cellular protein of Chlamydomonas reinhardtii (3) and Synechococcus PCC 7942 (4) isolated with PEB (AS08 300) were separated on 4-12% Nupage Bis-Tris gels in in MES running buffer (Invitrogen) at 200V for 35 minutes. Proteins were transferred for 80 minutes at 30V to a PVDF membrane pre-wetted in methanol and equilibrated in 1X transfer buffer. Blots were blocked immediately following transfer in 2% ECL Advance blocking reagent (GE Healthcare) in 20 mM Tris, 137 mM sodium chloride pH 7.6 with 0.1% (v/v) Tween-20 (TBS-T) and probed with anti-PsaH (AS06 143, 1:10000) and secondary HRP-conjugated goat anti-rabbit antibody (1:50 000, Abcam) for 1 hr in TBS-T containing 2% ECL Advance blocking reagent (GE Healthcare). Antibody incubations were followed by washings in TBS-T (15, +5, +5, +5 min). All steps were performed at RT with agitation. Signals was detected after 3 s using ECL Advance detection reagent (GE Healthcare) according to the manufacturers instructions and a CCD imager (FluorSMax, Bio-Rad)


  western blot detection using PsaH antibody

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