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Key Documents

R3757

Sigma-Aldrich

Reactive Yellow 3−Agarose

saline suspension

Synonym(s):

C.I.13245

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About This Item

MDL number:
UNSPSC Code:
23151817
NACRES:
NA.56

form

saline suspension

Quality Level

extent of labeling

1-5 mg per mL

matrix

cross-linked 4% beaded agarose

capacity

≥500 units/mL binding capacity (citrate synthase)

storage temp.

2-8°C

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Application

Reactive Yellow 3-agarose is used in affinity chromatography, protein chromatography and dye resins. Reactive Yellow 3-agarose has been used in immunohistochemical localization studies to show where tyramine N-(hydroxycinnamoyl)transferase (THT) polypeptides occur in opium poppy. Reactive Yellow-agarose has also been used to purify human cholesteryl ester transfer protein.

Physical form

Suspension in 0.5 M NaCl containing preservative

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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M L Fonda
The Journal of biological chemistry, 267(22), 15978-15983 (1992-08-05)
Human erythrocytes rapidly convert vitamin B6 to pyridoxal-P and contain soluble phosphatase activity which dephosphorylates pyridoxal-P at a pH optimum of 6-6.5. This phosphatase was purified 51,000-fold with a yield of 39% by ammonium sulfate precipitation and chromatography on DEAE-Sepharose
J M Stoop et al.
Archives of biochemistry and biophysics, 298(2), 612-619 (1992-11-01)
A mannitol:mannose 1-oxidoreductase was isolated from celeriac (Apium graveolens var. rapaceum) root tips by fractionation with (NH4)2SO4, followed by chromatography on a Fractogel DEAE column and then concentration with (NH4)2SO4. This newly discovered mannitol dehydrogenase catalyzes the NAD-dependent oxidation of
Purification of hydroxycinnamoyl-CoA:tyramine hydroxycinnamoyltransferase from cell-suspension cultures of <I>Solanum tuberosum</I> L. cv. Datura.
Hohlfeld, H., et al.
Planta, 199(1), 166-168 (1996)
X B Yi et al.
Biochimica et biophysica acta, 1310(3), 334-342 (1996-02-29)
Nucleoside diphosphate kinase (NDPK) participates in multiple cellular functions, yet the molecular mechanisms of its involvement are often unknown, given that there are no specific inhibitors for the enzyme from vertebrates. We developed antibodies against NDPK by immunization of rabbits
T Vogt et al.
Planta, 203(3), 349-361 (1997-01-01)
Uridine 5'-diphosphoglucose:betanidin 5-O- and 6-O-glucosyltransferases (5-GT and 6-GT; EC 2.4.1) catalyze the regiospecific formation of betanin (betanidin 5-O-beta-glucoside) and gomphrenin I (betanidin 6-O-beta-glucoside), respectively. Both enzymes were purified to near homogeneity from cell-suspension cultures of Dorotheanthus bellidiformis, the 5-GT by

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