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A3765

Sigma-Aldrich

N-(p-Aminophenyl)oxamic acid–Agarose

saline suspension

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About This Item

MDL number:
MFCD00801310
UNSPSC Code:
23151817
NACRES:
NA.56
Pricing and availability is not currently available.

form

saline suspension

Quality Level

200

matrix

cross-linked 4% beaded agarose

matrix activation

cyanogen bromide

matrix attachment

amino

matrix spacer

20 atoms

capacity

≥37 units/mL binding capacity (neuraminidase (N2876, 4MU-NANA substrate))

storage temp.

2-8°C

SMILES string

[X]Nc1ccc(cc1)NC(=O)C(=O)O

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feature

Holds 72 x 16-mm tubes

feature

Holds 72 x 16-mm tubes

feature

Holds 72 x 16-mm tubes

feature

Holds 72 x 16-mm tubes

manufacturer/tradename

Nalgene® 5970-0316

manufacturer/tradename

Nalgene® 5970-0216

manufacturer/tradename

Nalgene® 5970-0016

manufacturer/tradename

Nalgene® 5970-0116

packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea

packaging

pack of 1 ea

L × W × H

248 mm × 127 mm × 70 mm

L × W × H

248 mm × 127 mm × 70 mm

L × W × H

248 mm × 127 mm × 70 mm

L × W × H

248 mm × 127 mm × 70 mm

color

blue

color

yellow

color

white

color

orange

Application

N-(p-Aminophenyl)oxamic acid agarose is used in affinity chromatography, protein chromatography and in specialty resins. N-(p-Aminophenyl)oxamic acid has been used in studies characterizing sialidase, neuraminidase, β-N-acetylhexosaminidases and β-galactosidase.

Physical form

Suspension in 0.1 M NaCl containing preservative

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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    Certificates of Analysis (COA)

    Lot/Batch Number
    SLBW2464
    SLBT6825
    SLBS1922V
    SLBC4764V
    021M5164V

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    T Kiyohara et al.
    Journal of biochemistry, 80(1), 9-17 (1976-07-01)
    Three beta-N-acetylhexosaminidases [EC 3.2.1.52] and one beta-galactosidase [EC 3.2.1.23] were purified from the culture filtrate of streptococcus 6646 group K by a combination of column chromatographies on p-aminophenyl beta-D-thiogalactopyranoside-substituted Sepharose and N-(paminophenyl)oxamic acid-substituted Sepharose. These beta-N-acetylhexosaminidases showed optimal activities between
    X G Chen et al.
    European journal of biochemistry, 221(2), 655-664 (1994-04-15)
    Sialidase activities of rabbit blood cells and serum were measured. The leucocyte particulate fraction showed the highest specific activity of sialidase towards mixed gangliosides and sialyllactose, and the cytosolic fraction showed for fetuin. Predominant sialidase activity in the blood was
    A Varki et al.
    The Journal of biological chemistry, 258(20), 12465-12471 (1983-10-25)
    The naturally occurring sialic acids can have different types of N- and O-substitutions, resulting in more than 20 known isomers and compounds. Most methods for the detailed study of these various sialic acids require that the molecules be first released

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