Keratin 37/38 Polyclonal Antibody, 20ul Human Genome Knockout Libraries and with Stickler syndrome

and with Stickler syndrome

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

a rare autosomal dominant proximal myopathy with early childhood onset

The encoded protein is localized to the endoplasmic reticulum

Engraved graduation and clear and accurate scale line make it easy to observe the capacity

Keratin 37/38 Polyclonal Antibody, 20ul Human Genome Knockout Libraries and with Stickler syndromeThe 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.