Amnionless (AMN) ELISA试剂盒

The protein encoded by AMN is a type I transmembrane protein. 再加上,我们可以发AMN 蛋白 (8)AMN 抗体 (6)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
AMN 81693 Q9BXJ7
AMN 93835 Q99JB7
AMN    

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产品编号 适用 灵敏度 范围 图像 规格 供应商 交付 价格 详细
大鼠 0.214 ng/mL 0.62-40 ng/mL 96 Tests Log in to see 7至10个工作日
¥3,772.08
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0.107 ng/mL 0.312-20 ng/mL 96 Tests Log in to see 9至11个工作日
¥4,293.90
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小鼠 3.9 pg/mL Typical standard curve 96 Tests Log in to see 9至12个工作日
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适于 AMN 相互作用对的更多 ELISA 试剂盒

Human Amnionless (AMN) interaction partners

  1. 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

  2. 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).

  3. amnionless is essential for the correct luminal expression of cubilin (显示 CUBN ELISA试剂盒) in humans.

  4. homozygous mutations affecting exons 1-4 of human AMN (显示 ABCD1 ELISA试剂盒) lead to megaloblastic anemia 1

  5. 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

  6. Recurrent spontaneous abortions may be caused by mutations in the Amnionless gene.

  7. This review summarizes recent data on the biological function of amnionless and focuses on its implication in embryonic nutrition and central nervous system malformations.

Mouse (Murine) Amnionless (AMN) interaction partners

  1. 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

  2. Amn (显示 TRAF3 ELISA试剂盒) is an essential component of the Cubn (显示 CUBN ELISA试剂盒) receptor complex

AMN 抗原简介

Antigen Summary

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.

Gene names and symbols associated with Amnionless (AMN) ELISA试剂盒

  • amnionless homolog (amn) 抗体
  • amnion associated transmembrane protein (AMN) 抗体
  • amnionless (Amn) 抗体
  • amnionless homolog (mouse) (AMN) 抗体
  • 5033428N14Rik 抗体
  • amnionless 抗体
  • AV002116 抗体
  • MGC81896 抗体
  • PRO1028 抗体

Protein level used designations for Amnionless (AMN) ELISA试剂盒

amnionless homolog , protein amnionless , visceral endoderm-specific type 1 transmembrane protein , type I transmembrane protein

GENE ID SPECIES
444498 Xenopus laevis
81693 Homo sapiens
93835 Mus musculus
403434 Canis lupus familiaris
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