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S6A19 Polyclonal Antibody, 50ul Nucleic Acid Amplification Deficiency in this protein (B-cell

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S6A19 Polyclonal Antibody, 50ul Nucleic Acid Amplification Deficiency in this protein (B-cellThis gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder.

Store: matisco.be · Domain: matisco.be

Description

Deficiency in this protein (B-cell linker)has also been shown in some cases of pre-B acute lymphoblastic leukemia

These multimeric G-protein-gated inwardly-rectifying potassium (GIRK) channels may play a role in the pathophysiology of epilepsy

cytoplasmic proteins that bind long-chain fatty acids and other hydrophobic ligands

The protein encoded by this gene is a member of the 7 transmembrane-spanning G protein-coupled receptor family

S6A19 Polyclonal Antibody, 50ul Nucleic Acid Amplification Deficiency in this protein (B-cellThis gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder.

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