PsbP | 23 kDa protein of the oxygen evolving complex (OEC) of PSII (anti-monocot protein)

Name: PsbP | 23 kDa protein of the oxygen evolving complex (OEC) of PSII (anti-monocot protein)
SKU: AS08 305
Price: 394 EUR
Availability: InStock

AS08 305 | Clonality: Polyclonal | Host: Rabbit | Reactivity: A. thaliana, S. bicolor, Z. mays

PsbP | 23 kDa protein of the oxygen evolving complex (OEC) of PSII (anti-monocot protein) in the group Antibodies Plant/Algal / Photosynthesis / PSII (Photosystem II) at Agrisera AB (Antibodies for research) (AS08 305)

PsbP | 23 kDa protein of the oxygen evolving complex (OEC) of PSII (anti-monocot protein)

Product Information

Immunogen

Recombinant sorghum OE23 protein

Host Rabbit

Clonality Polyclonal

Purity Serum

Format Lyophilized

Quantity 100 µl

Reconstitution For reconstitution add 100 µl of sterile water

Storage Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.

Tested applications Western blot (WB)

Recommended dilution 1 : 5 000 (WB)

Expected | apparent MW

23 kDa

Reactivity

Confirmed reactivity Arabidopsis thaliana, Sorghum bicolor, Zea mays

Predicted reactivity Hordeum vulgare, Oryza sativa
Species of your interest not listed? Contact us

Not reactive in No confirmed exceptions from predicted reactivity are currently known

Application examples

Application examples Application example

AS08 305 PsbP western.jpg

5 µg of total protein from (1) Arabidopsis thaliana total leaf extract; (2) Zea mays total leaf extract were separated in a 12% or 5-15% gradient gel following by transfer to nitrocellulose membrane. Membrane was blocked with TBST + 4% non-fat dried milk, 20 min following by three washes in TBST. Incubation time with primary and secondary antibodies was 1 hr primary, 30 min for secondary antibodies. Dectetion was performed using chemiluminescence.

Additional information

Background

PSII reaction centre components are generating the redox potential required to drive highly oxidizing water splitting reaction. Four Mn atoms are present on a lumenal surface and form the catalyctic site of the water-splitting reaction which is in close association with the 33 kDa (PsbO), 23 kDa (PsbP) and 17 kDa (PsbQ) extrinistic subunits of oxygen evolving complex OEC. A 33-kDa extrinsic protein is also termed the Mn-stabilizing protein (MSP), however recent evidences shown that it is C-terminal domain of PsbA (D1) protein which is involved in in the assembly and stabilization of the OEC.

Product citations

immunogen:	Recombinant sorghum OE23 protein
Reconstitution:	For reconstitution add 100 µl of sterile water
Host:	Rabbit
Clonality:	Polyclonal
Purity:	Serum
Format:	Lyophilized
Quantity:	100 µl
storage:	Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.
tested applications:	Western blot (WB)
recommended dilution:	1 : 5 000 (WB)
calculated \| apparent molecular mass [kDa]:	23 kDa
Confirmed reactivity:	Arabidopsis thaliana, Sorghum bicolor, Zea mays
predicted reactivity:	Hordeum vulgare, Oryza sativa Species of your interest not listed? Contact us
not reactive in:	No confirmed exceptions from predicted reactivity are currently known
Picture (footer):	Application example 5 µg of total protein from (1) Arabidopsis thaliana total leaf extract; (2) Zea mays total leaf extract were separated in a 12% or 5-15% gradient gel following by transfer to nitrocellulose membrane. Membrane was blocked with TBST + 4% non-fat dried milk, 20 min following by three washes in TBST. Incubation time with primary and secondary antibodies was 1 hr primary, 30 min for secondary antibodies. Dectetion was performed using chemiluminescence.
background:	PSII reaction centre components are generating the redox potential required to drive highly oxidizing water splitting reaction. Four Mn atoms are present on a lumenal surface and form the catalyctic site of the water-splitting reaction which is in close association with the 33 kDa (PsbO), 23 kDa (PsbP) and 17 kDa (PsbQ) extrinistic subunits of oxygen evolving complex OEC. A 33-kDa extrinsic protein is also termed the Mn-stabilizing protein (MSP), however recent evidences shown that it is C-terminal domain of PsbA (D1) protein which is involved in in the assembly and stabilization of the OEC.

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