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A2278

N-Acetyl-D-glucosamine–Agarose

saline suspension

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NACRES:
NA.56
PubChem Substance ID:
UNSPSC Code:
41106500
MDL number:
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form

saline suspension

Quality Level

matrix

6% beaded agarose

matrix activation

divinyl sulfone

matrix attachment

hydroxyl

matrix spacer

5 atoms

capacity

≥25 mg/mL binding capacity (Triticum vulgaris lectin)

storage temp.

2-8°C

SMILES string

CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO

InChI

1S/C8H15NO6/c1-4(12)9-5(2-10)7(14)8(15)6(13)3-11/h2,5-8,11,13-15H,3H2,1H3,(H,9,12)/t5-,6+,7+,8+/m0/s1

InChI key

MBLBDJOUHNCFQT-LXGUWJNJSA-N

General description

N-Acetyl-D-glucosamine is used in affinity chromatography, protein chromatography, and carbohydrate matrices. N-Acetyl-D-glucosamine can be used to purify wheat germ (Triticum vulgaris) lectin.

Application

N-Acetyl-D-glucosamine-Agarose has been used

  • for the incubation of supernatant for the depletion of ficolin-3-deficient serum[1]
  • for detecting the lectin activity by ligand binding assays[2]
  • to produce ficolin 2 depleted serum[3]

Physical form

Suspension in 0.15 M NaCl, 0.01 M sodium phosphate, pH 6.8, containing 0.02% sodium azide

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Este artículo
G5509A32861079
Quality Level

200

Quality Level

300

Quality Level

200

Quality Level

100

form

saline suspension

form

powder

form

powder

form

powder

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

matrix spacer

5 atoms

matrix spacer

-

matrix spacer

-

matrix spacer

-

matrix

6% beaded agarose

matrix

-

matrix

-

matrix

-

matrix activation

divinyl sulfone

matrix activation

-

matrix activation

-

matrix activation

-


Clase de almacenamiento

10 - Combustible liquids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable



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Comparative Biochemistry of Molecular Targets for Drug and Pesticides: N-acetyl-D-glucosamine and Acetylcholine Related Enzymes
Yang, Q.Y.
Current Drug Targets (2012)
M B Allen et al.
The Biochemical journal, 185(3), 577-582 (1980-03-01)
1. Under normal assay conditions the N-acetyl-D-glucosamine kinases from rat liver and kidney show a pH-dependent lag phase before reaching a steady state, which is probably due to reversible dissociation of the dimeric enzyme. 2. The enzyme catalyses the phosphorylation
M B Allen et al.
The Biochemical journal, 185(3), 565-575 (1980-03-01)
1. Procedures for the extensive purification in high yield of N-acetyl-D-glucosamine kinase from rat liver and kidney are described. The separation of this enzyme from hepatic glucokinase depended primarily on their differing behaviour on an affinity column of Sepharose--N-(6-aminohexanoyl)-2-amino-2-deoxy-D-glucopyranose. 2.



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SKUGTIN
A2278-1ML04061837765582
A2278-5ML04061833349960
A2278-25ML04061837765599

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