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In humans endoglin may be involved in the autosomal dominant disorder known as hereditary hemorrhagic telangiectasia (HHT) type 1
atrial flutter
PYWTNTEKMEKRLHAVPAANTVKFRCPAGGNPMPTMRWLKNGKEFKQEHRIGGYKVRNQHWSLIMESVVPSDKGNYTCVVENEYGSINHTYHLDVVERSPHRPILQAGLPANASTVVGGDVEFVCKVYSDAQPHIQWIKHVEKNGSKYGPDGLPYLKVLKHSGINSSNAEVLALFNVTEADAGEYICKVSNYIGQANQSAWLTVLGGGSGGGSHHHHHHHHHH
Prolactin (PRL)
add 10 mL passage buffer
GARP&Latent TGF-β1 Heterotrimer His Tag Protein, Human IHC Kits In humans endoglin may beProduct Specification Species Human Synonyms RRC32 & TGF beta 1, LRRC32&TGFB1 Accession Q14392P01137 Amino Acid Sequence GARP: His20 Asn627, with C terminal 10*His
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