HBA Polyclonal Antibody, 100ul Multi-Layer Cell Culture System Defects in this gene are

Defects in this gene are the cause of hemochromatosis type 2A

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This protein plays a role in diverse developmental contexts

The encoded protein suppresses anchorage-dependent growth and promotes cell migration and adhesion through interactions with the actin cytoskeleton via the PDZ domain

A non-transcribed pseudogene of GnRHR2 is located on chromosome 14

HBA Polyclonal Antibody, 100ul Multi-Layer Cell Culture System Defects in this gene areThe human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5' zeta pseudozeta mu pseudoalpha 1 alpha 2 alpha 1 theta 3'. The alpha 2 (HBA2) and alpha 1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult