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Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B
Immunogen: A synthesized peptide derived from human CtBP1
Immunogen: The antiserum was produced against synthesized peptide derived from human ZP4
and Axenfeld-Rieger anomaly
AF0514-200
PCK1 Polyclonal Antibody - E-AB-60569 K4 System Mucopolysaccharidosis type VI is anPCK1 Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 60569 60, E AB 60569 120, E AB 60569 200 Citations, Manuals and MSDS Available upon request. Abbreviation: PCK1 Target Synonym: PCK1; PEPCK C; PEPCK1; PEPCKC Research Areas: Cancer, Cardiovascular, Metabolism, Signal Transduction Conjugation: Unconjugated Host: Rabbit Species Reactivity: Human, Mouse, Rat Application: WB Isotype: IgG Clonality: Polyclonal UNIProt ID: P35558
US$ 12.00
US$ 12.00
US$ 12.00
US$ 12.00