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多克隆抗體

FA73A rabbit Polyclonal Antibody

FA73A抗體
FA73A抗體應(yīng)用:WB 1:500-2000

FA78A rabbit Polyclonal Antibody

FA78A抗體
FA78A抗體應(yīng)用:WB 1:500-2000

FA78B rabbit Polyclonal Antibody

FA78B抗體
FA78B抗體應(yīng)用:WB 1:500-2000

FA81B rabbit Polyclonal Antibody

FA81B抗體
FA81B抗體應(yīng)用:WB 1:500-2000

FA86A rabbit Polyclonal Antibody

FA86A抗體
FA86A抗體應(yīng)用:WB 1:500-2000

FA86C rabbit Polyclonal Antibody

FA86C抗體
FA86C抗體應(yīng)用:WB 1:500-2000

FA89A rabbit Polyclonal Antibody

FA89A抗體
FA89A抗體應(yīng)用:WB 1:500-2000

FA98B rabbit Polyclonal Antibody

FA98B抗體
FA98B抗體應(yīng)用:WB 1:500-2000

FABP9 rabbit Polyclonal Antibody

FABP9抗體
FABP9抗體應(yīng)用:WB 1:500-2000

FACR1 rabbit Polyclonal Antibody

FACR1抗體
FACR1抗體應(yīng)用:WB 1:500-2000 The protein encoded by this gene is required for the reduction of fatty acids to fatty alcohols, a process that is required for the synthesis of monoesters and ether lipids. NADPH is required as a cofactor in this reaction, and 16-18 carbon saturated and unsaturated fatty acids are the preferred substrate. This is a peroxisomal membrane protein, and studies suggest that the N-terminus contains a large catalytic domain located on the outside of the peroxisome, while the C-terminus is exposed to the matrix of the peroxisome. Studies indicate that the regulation of this protein is dependent on plasmalogen levels. Mutations in this gene have been associated with individuals affected by severe intellectual disability, early-onset epilepsy, microcephaly, congenital cataracts, growth retardation, and spasticity (PMID: 25439727). A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jan 2015],
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