Use your antibodies-online credentials, if available.
The protein encoded by AMN is a type I transmembrane protein. 再加上，我们可以发AMN 蛋白 (8) 和 AMN 抗体 (6)和数多这个蛋白质的别的产品。
Showing 4 out of 14 products:
Human AMN ELISA Kit for Sandwich ELISA - ABIN418006
Pannérec, Migliavacca, De Castro, Michaud, Karaz, Goulet, Rezzi, Ng, Bosco, Larbi, Feige: Vitamin B12 deficiency and impaired expression of amnionless during aging. in Journal of cachexia, sarcopenia and muscle 2017
heterozygous mutations in AMN (显示 ABCD1 ELISA试剂盒) 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 (显示 CUBN ELISA试剂盒), AMN (显示 ABCD1 ELISA试剂盒), and GIF (显示 GIF ELISA试剂盒).
amnionless is essential for the correct luminal expression of cubilin (显示 CUBN ELISA试剂盒) in humans.
homozygous mutations affecting exons 1-4 of human AMN (显示 ABCD1 ELISA试剂盒) lead to megaloblastic anemia 1
cubilin (显示 CUBN ELISA试剂盒) and amnionless are subunits of a novel cubilin (显示 CUBN ELISA试剂盒)/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 (显示 TRAF3 ELISA试剂盒) 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 (显示 TRAF3 ELISA试剂盒) is an essential component of the Cubn (显示 CUBN ELISA试剂盒) 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