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F5875

Sigma-Aldrich

Ferredoxin from Spinacia oleracea (spinach)

buffered aqueous solution

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About This Item

CAS Number:
9040-09-9
MDL number:
MFCD00131049
UNSPSC Code:
12352202
NACRES:
NA.61
Pricing and availability is not currently available.

biological source

spinach (Spinacia oleracea)

Quality Level

200

form

buffered aqueous solution

concentration

1.0-3.0 mg/mL in 0.15 M Trizma buffer, pH 7.5 and NaCl (Frozen)

application(s)

cell analysis

shipped in

dry ice

storage temp.

−70°C

Gene Information

spinach ... SOVF(137530)

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This Item
F3013F6879F7879
Ferredoxin from Spinacia oleracea (spinach) buffered aqueous solution

F5875

Ferredoxin from Spinacia oleracea (spinach)

Ferredoxin from Spinacia oleracea (spinach) lyophilized powder, Ferredoxin ≥15 wt. %

F3013

Ferredoxin from Spinacia oleracea (spinach)

Ferritin from human spleen Type V, 10 μg/mL in 0.15 M NaCl, 10 mM Tris, pH 8.0, containing 0.1% sodium azide

F6879

Ferritin from human spleen

Ferritin, cationized from horse spleen 10 mg/mL in 0.15 M NaCl

F7879

Ferritin, cationized from horse spleen

biological source

spinach (Spinacia oleracea)

biological source

spinach (Spinacia oleracea)

biological source

human spleen

biological source

horse spleen

concentration

1.0-3.0 mg/mL in 0.15 M Trizma buffer, pH 7.5 and NaCl (Frozen)

concentration

-

concentration

10 μg/mL in 0.15 M NaCl, 10 mM Tris, pH 8.0, containing 0.1% sodium azide

concentration

10 mg/mL in 0.15 M NaCl

form

buffered aqueous solution

form

lyophilized powder

form

liquid

form

liquid

storage temp.

−70°C

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

2-8°C

shipped in

dry ice

shipped in

-

shipped in

-

shipped in

-

Gene Information

spinach ... SOVF(137530)

Gene Information

spinach ... SOVF(137530)

Gene Information

human ... FTH1(2495), FTL(2512)

Gene Information

horse ... FTL(100051593)

Application

Ferredoxin has been used in studies of assimilation of inorganic nitrogen from nitrite or nitrate in the absence of ammonium. Ferredoxin is important in the electron transfer cascade required for this nitrogen assimilation.

Biochem/physiol Actions

Ferredoxins are iron-containing proteins that serve as electron-transfer catalysts in photosynthesis and nitrogen fixation.

Packaging

Package sizes are based on ferredoxin content.

Preparation Note

Partially purified by the method of Tagawa and Arnon, Nature, 195, 537 (1962).

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SLCG9732
SLCD4171
SLBX7845
SLBT6942
SLBM1758V

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C K Derian et al.
The Journal of biological chemistry, 264(12), 6615-6618 (1989-04-25)
While a role has been ascribed to the gamma-carboxyglutamate (Gla) residues in vitamin K-dependent coagulation proteins and the enzyme catalyzing this posttranslational modification has been identified and partially characterized, both the functional significance of a second posttranslationally synthesized amino acid
H M Rowe et al.
Applied spectroscopy, 57(5), 532-537 (2003-12-09)
An adaptation of square-wave gated phase-modulation (GPM) fluorimetry allows for self-referenced intensity measurements without the complexity of dual excitation or dual emission wavelengths. This AC technique utilizes square-wave excitation, gated detection, a reference emitter, and a sensor molecule. The theory
Michael Raghunath et al.
Biochemical and biophysical research communications, 378(4), 766-771 (2008-12-11)
The rapid vascularisation of biomaterials and engineered tissue after implantation is a current unmet need. To this end, we explored the pharmacological option of inducing neovascularisation using compounds that inhibit hypoxia-induced factor-1alpha prolyl hydroxylase. This stabilises hypoxia inducible factor-1alpha and
John R G Sander et al.
Journal of pharmaceutical sciences, 99(9), 3676-3683 (2010-06-25)
We report on a co-crystal of acetaminophen (APAP) and 2,4-pyridinedicarboxylic acid (PDA). The co-crystal was discovered by screening using the solution-mediated phase transformation (SMPT) technique. Despite the bulk solids of each component being white in color, the new co-crystal phase
Guo-liang Gu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(1), 209-214 (2008-02-19)
Two novel ligands containing two pyridine-2,6-dicarboxylic acid conjugative units, 4-(2-(2,6-dicarbox-ypyridin-4-yl)vinyl)pyridine-2,6-dicarboxylic acid (L1) and 4-(4-(2-(2,6-dicarboxypyridin-4-yl)vinyl)styryl)pyridine-2,6-dicarboxylic acid (L2) and their complexes with Tb(III) have been synthesized and characterized by elemental analysis, IR spectra and NMR. The ligand synthetic route was optimized and
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