Anti-Human IDS Monoclonal Antibody

Categories: [ Antibodies][ Monoclonal Antibodies]

Iduronate 2-sulfatase (IDS) is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations causing IDS deficiency in humans result in the lysosomal storage of these glycosaminoglycans and Hunter syndrome,an X chromosome-linked disease. An internal proteolytic cleavage occurs to produce the mature IDS present in human liver shown to contain a 42 kDa polypeptide N-terminal to a 14 kDa polypeptide..

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Properties

Data Sheet	Click for Datasheet
Catalog Number	MA01999
Size	100μl
Host Type	Mouse
Immunogen	Fusion protein of Iduronate 2 sulfatase
Specificity	Liver, kidney, lung, and placenta.
Isotype	IgG1
Reacitivity	Human
Clone	3210
Uniprot	P22304
Concentration	None
Dilution	WB 1:200-1:2000, IHC 1:20-1:200, IF 1:20-1:200
Formulation
Application	WB,IHC,IF,ELISA
Other Names	Alpha L iduronate sulfate sulfatase,Alpha-L-iduronate sulfate sulfatase,AW214631,Ids,IDS,Iduronate 2 sulfatase 14 kDa chain,Iduronate 2 sulfatase 42 kDa chain,Iduronate 2 sulfatase,Iduronate 2-sulfatase 14 kDa chain,Iduronate sulfatase,Idursulfase,MPS2,RP23-29M4.1,SIDS
Storage	Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript	For research use only, not for use in diagnostic procedures.

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Anti-Human IDS Monoclonal Antibody

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