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The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. SLC33A1 Polyclonal Antibody Codice: E-AB-12874_120μL Confezionamento: 120μL	Dettagli
The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. SLC33A1 Polyclonal Antibody Codice: E-AB-12874_60μL Confezionamento: 60μL	Dettagli
The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. SLC33A1 Polyclonal Antibody Codice: E-AB-12874_20μL Confezionamento: 20μL	Dettagli
The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. SLC33A1 Polyclonal Antibody Codice: E-AB-16066_200μL Confezionamento: 200μL	Dettagli
The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. SLC33A1 Polyclonal Antibody Codice: E-AB-16066_120μL Confezionamento: 120μL	Dettagli
The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. SLC33A1 Polyclonal Antibody Codice: E-AB-16066_20μL Confezionamento: 20μL	Dettagli
The protein encoded by this gene is required for the formation of O-acetylated (Ac) gangliosides. The encoded protein is predicted to contain 6 to 10 transmembrane domains, and a leucine zipper motif in transmembrane domain III. Defects in this gene have been reported to cause spastic paraplegia autosomal dominant type 42 (SPG42) in one Chinese family, but not in similar patients of European descent. Two transcript variants encoding the same protein have been found for this gene. SLC33A1 Polyclonal Antibody Codice: E-AB-16066_60μL Confezionamento: 60μL	Dettagli
A synthesized peptide derived from human SLC34A1. SLC34A1 Antibody Codice: DF15316 Confezionamento: 100ul	Dettagli
A synthesized peptide derived from human SLC34A2, corresponding to a region within N-terminal amino acids. SLC34A2 Antibody Codice: DF2244 Confezionamento: 100ul	Dettagli
The protein encoded by this gene is a pH-sensitive sodium-dependent phosphate transporter. Phosphate uptake is increased at lower pH. Defects in this gene are a cause of pulmonary alveolar microlithiasis. Three transcript variants encoding two different isoforms have been found for this gene. SLC34A2 Polyclonal Antibody Codice: E-AB-12644_60μL Confezionamento: 60μL	Dettagli
The protein encoded by this gene is a pH-sensitive sodium-dependent phosphate transporter. Phosphate uptake is increased at lower pH. Defects in this gene are a cause of pulmonary alveolar microlithiasis. Three transcript variants encoding two different isoforms have been found for this gene. SLC34A2 Polyclonal Antibody Codice: E-AB-12644_20μL Confezionamento: 20μL	Dettagli
The protein encoded by this gene is a pH-sensitive sodium-dependent phosphate transporter. Phosphate uptake is increased at lower pH. Defects in this gene are a cause of pulmonary alveolar microlithiasis. Three transcript variants encoding two different isoforms have been found for this gene. SLC34A2 Polyclonal Antibody Codice: E-AB-12644_200μL Confezionamento: 200μL	Dettagli

1…16759 16760 167611676216763 16764 16765…19204

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