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The protein encoded by AMN is a type I transmembrane protein. Additionally we are shipping AMN Proteins (8) and AMN Antibodies (4) and many more products for this protein.
Showing 4 out of 10 products:
heterozygous mutations in AMN (show ABCD1 ELISA Kits) in a family from the United Kingdom with clinical features of Imerslund-Grasbeck Syndrome
Our genetic screening of 154 families of patients with inherited cobalamin malabsorption revealed population-specific mutations, mutational hotspots, and functionally distinct regions in the three causal genes: CUBN (show CUBN ELISA Kits), AMN (show ABCD1 ELISA Kits), and GIF (show GIF ELISA Kits).
amnionless is essential for the correct luminal expression of cubilin (show CUBN ELISA Kits) in humans.
homozygous mutations affecting exons 1-4 of human AMN (show ABCD1 ELISA Kits) lead to megaloblastic anemia 1
cubilin (show CUBN ELISA Kits) and amnionless are subunits of a novel cubilin (show CUBN ELISA Kits)/amnionless (cubam) complex
Recurrent spontaneous abortions may be caused by mutations in the Amnionless gene.
This review summarizes recent data on the biological function of amnionless and focuses on its implication in embryonic nutrition and central nervous system malformations.
AMN (show TRAF3 ELISA Kits) may participate in meiosis in early spermatocytes and in functional differentiation of adult Leydig cells through the mediation of vitamin B(12) transport in the mouse testes
Amn (show TRAF3 ELISA Kits) is an essential component of the Cubn (show CUBN ELISA Kits) receptor complex
The protein encoded by this gene is a type I transmembrane protein. It is thought to modulate bone morphogenetic protein (BMP) receptor function by serving as an accessory or coreceptor, and thus facilitates or hinders BMP binding. It is known that the mouse AMN gene is expressed in the extraembryonic visceral endoderm layer during gastrulation, but it is found to be mutated in amnionless mouse. The encoded protein has sequence similarity to short gastrulation (Sog) and procollagen IIA proteins in Drosophila.
, protein amnionless
, visceral endoderm-specific type 1 transmembrane protein
, type I transmembrane protein