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Bis-hydrazide modification

Most proteins contain an abundance of carboxylic acid groups from C-terminal functionalities and aspartic and glutamic acid side chains. These groups are readily modified with bis-hydrazide compounds to yield useful hydrazide-activated derivatives. Both carbohydrazide and adipic acid dihydrazide have been employed in forming these modifications using the carbodi-imide reaction (Wilchek and Bayer, 1987). [Pg.142]

The following protocol describes the modification of DNA or RNA probes at their 5 -phosphate ends with a bis-hydrazide compound, such as adipic acid dihydrazide or carbohydrazide. A similar procedure for coupling the diamine compound cystamine can be found in Section 2.2 (this chapter). [Pg.980]


See other pages where Bis-hydrazide modification is mentioned: [Pg.974]    [Pg.664]    [Pg.644]    [Pg.974]    [Pg.664]    [Pg.644]    [Pg.146]    [Pg.613]    [Pg.974]    [Pg.141]    [Pg.143]    [Pg.144]    [Pg.145]    [Pg.664]    [Pg.121]    [Pg.123]    [Pg.124]    [Pg.125]    [Pg.644]    [Pg.124]   
See also in sourсe #XX -- [ Pg.644 ]

See also in sourсe #XX -- [ Pg.644 ]




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Hydrazide modification

Modification bis-hydrazides

Modification bis-hydrazides

Modification hydrazides

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