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CPT2 Rabbit Polyclonal Antibody, 50ul Transporters Mutations in this gene are

SKU: 9144153587

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CPT2 Rabbit Polyclonal Antibody, 50ul Transporters Mutations in this gene are

Store: gaabil.dk · Domain: gaabil.dk

Description

Mutations in this gene are associated with type II autosomal recessive Alport syndrome (hereditary glomerulonephropathy) and with familial benign hematuria (thin basement membrane disease)

and miRNA-200b is itself downregulated in glioma tissues

opsin subfamily

This protein is a member of the White subfamily and is expressed predominantly in liver tissue

This secreted protease (matrix metallopeptidase 1) breaks down the interstitial collagens

CPT2 Rabbit Polyclonal Antibody, 50ul Transporters Mutations in this gene are

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