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F0628

Ferredoxin-NADP+ Reductase from Spinacia oleracea (spinach)

lyophilized powder, ≥15 units/mg solid, secondary activity: ≥10 units/mg solid NADPH diaphorase

Synonym(s):

Ferridoxin-NADP+ oxidoreductase

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1 UNIT

$150.00

5 UNITS

$519.00

10 UNITS

$942.00

$150.00


Estimated to ship onAugust 31, 2026Details



About This Item

CAS Number:
EC Number:
UNSPSC Code:
12352204
NACRES:
NA.54
MDL number:
Specific activity:
≥15 units/mg solid

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form

lyophilized powder

specific activity

≥15 units/mg solid

foreign activity

NADH diaphorase activity ≤10 units/mg solid

storage temp.

−20°C

Quality Level

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This Item
F3013P9752F5875
specific activity

≥15 units/mg solid

specific activity

-

specific activity

≥40 units/mg protein (biuret)

specific activity

-

form

lyophilized powder

form

lyophilized powder

form

partially purified powder

form

buffered aqueous solution

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−70°C

foreign activity

NADH diaphorase activity ≤10 units/mg solid

foreign activity

-

foreign activity

-

foreign activity

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

General description

Ferredoxin-NADP+ Reductase is a ferredoxin-soluble partner with a molar ratio to PSI of 0.9 and 3.[1]

Application

Ferredoxin-NADP+ Reductase from Spinacia oleracea (spinach) has been used to test the effect of potential protein partners on the activity of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH)−CP12 preparation.[2] It has also been used in standard assay conditions for phycocyanobilin:ferredoxin oxidoreductase (PcyA) enzyme assay.[3]
Ferredoxin-NADP+ Reductase was used in in vitro ferredoxin-dependent desaturation of fatty acids in cyanobacterial thylakoid membranes.[4] It was also used to regulate glyceraldehyde-3-phosphate dehydrogenase.[5]

Biochem/physiol Actions

Ferredoxin-NADP+ reductase catalyzes the reversible conversion of reduced ferredoxin to oxidized ferredoxin during photosynthesis.[6] Ferredoxin-NADP(H) reductase constitutes a family of hydrophilic FAD-containing monomeric enzymes that deliver NADPH or low potential one-electron donors to redox-based metabolisms in plastids, mitochondria, and bacteria.[7]
Ferredoxin-NADP+ reductase catalyzes the reversible conversion of reduced ferredoxin to oxidized ferredoxin during photosynthesis[6]. Ferredoxin-NADP(H) reductase constitutes a family of hydrophilic FAD-containing monomeric enzymes that deliver NADPH or low potential one-electron donors to redox-based metabolisms in plastids, mitochondria, and bacteria.

Other Notes

One unit will reduce 1.0 millimole of cytochrome C per min at pH 7.5 at 25 °C in the presence of spinach ferredoxin and NADP.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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[Laparocentesis in clinical traumatology].
V V Kuz'menko et al.
Khirurgiia, (6)(6), 50-54 (1986-06-01)
CRYSTALLIZATION OF FERREDOXIN-TPN REDUCTASE AND ITS ROLE IN THE PHOTOSYNTHETIC APPARATUS OF CHLOROPLASTS.
M SHIN et al.
Biochemische Zeitschrift, 338, 84-96 (1963-01-01)
Sara Baroni et al.
Biochemistry, 51(18), 3819-3826 (2012-04-24)
Plasmodium falciparum ferredoxin-NADP(+) reductase (FNR) is a FAD-containing enzyme that, in addition to be a promising target of novel antimalarial drugs, represents an excellent model of plant-type FNRs. The cofactor specificity of FNRs depends on differences in both k(cat) and
Shin, M.
Methods in Enzymology, 23, 441-441 (1971)
Manuel Twachtmann et al.
The Plant cell, 24(7), 2979-2991 (2012-07-19)
To adapt to different light intensities, photosynthetic organisms manipulate the flow of electrons through several alternative pathways at the thylakoid membrane. The enzyme ferredoxin:NADP(+) reductase (FNR) has the potential to regulate this electron partitioning because it is integral to most

Protocols

Enzymatic Assay of Ferredoxin NADP Reductase - To standardize a procedure for the enzymatic assay of Ferredoxin NADP Reductase (EC.1.18.12).

Questions

1–2 of 2 Questions  
  1. Hi, how can I prepare a stock solution with the 1 U vial? It's not very clear for me in the specification sheet. I need a 1 uM final concentration of reductase for my assay, how do I prepare a stock solution of it?

    1 answer
    1. The molecular weight of this enzyme has not been analyzed. The enzymatic assay states a solubility of 1 mg/ ml in water.
      Immediately prior to pipetting into cuvette, prepare a solution at 1 mg / mL in cold purified water. Place on ice.
      This solution is stable for a maximum of thirty minutes.

      Helpful?

  2. Hi there, could you please provide the specific methodology to extract this lyophilized powder from the vial? I didn't know how to extract this ferredoxin-NADP+ reductase from the vial

    1 answer
    1. The vials contain less than 1mg solid so reconstituting the whole vial is recommended.

      Helpful?

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