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Keratin 37/38 Polyclonal Antibody, 20ul Human Genome Knockout Libraries Mutations in the TFR2 gene

SKU: 69858322905

4.1
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Keratin 37/38 Polyclonal Antibody, 20ul Human Genome Knockout Libraries Mutations in the TFR2 geneThe protein encoded by KRT37 (keratin 37) is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12 q21 and have the same direction of transcription.

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Description

Mutations in the TFR2 gene result in hereditary hemochromatosis type III (HFE3)

and with Stickler syndrome

Schwann cells and fibroblasts

a rare autosomal dominant proximal myopathy with early childhood onset

Keratin 37/38 Polyclonal Antibody, 20ul Human Genome Knockout Libraries Mutations in the TFR2 geneThe protein encoded by KRT37 (keratin 37) is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12 q21 and have the same direction of transcription.

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