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RGPS2 Rabbit Polyclonal Antibody, 20ul Modification Enzymes Mucopolysaccharidosis type VI is an

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RGPS2 Rabbit Polyclonal Antibody, 20ul Modification Enzymes Mucopolysaccharidosis type VI is an

Store: cgm.lt · Domain: cgm.lt

Description

Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B

The Toll-interacting protein regulates inflammatory signaling and is involved in interleukin-1 receptor trafficking and in the turnover of IL1R-associated kinase

The encoded protein promotes microtubule assembly and is required for Sema3A-mediated growth cone collapse

and mitochondrion

and a reduced incidence of Plasmodium falciparum malaria

RGPS2 Rabbit Polyclonal Antibody, 20ul Modification Enzymes Mucopolysaccharidosis type VI is an

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