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anti-Amnionless (AMN) Antibodies

The protein encoded by AMN is a type I transmembrane protein. Additionally we are shipping AMN Kits (10) and AMN Proteins (8) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
AMN 81693 Q9BXJ7
Anti-Mouse AMN AMN 93835 Q99JB7
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Top anti-AMN Antibodies at antibodies-online.com

Showing 4 out of 5 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated WB 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB 50 μg Log in to see 8 to 10 Days
$551.83
Details
Human Rabbit Un-conjugated ICC, IF, IHC, IHC (p)   0.1 mL Log in to see 8 to 11 Days
$439.69
Details
Human Rabbit Un-conjugated ELISA, WB   100 μg Log in to see 9 to 14 Days
$417.00
Details

AMN Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human ,


More Antibodies against AMN Interaction Partners

Human Amnionless (AMN) interaction partners

  1. heterozygous mutations in AMN (show ABCD1 Antibodies) 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 (show CUBN Antibodies), AMN (show ABCD1 Antibodies), and GIF (show GIF Antibodies).

  3. amnionless is essential for the correct luminal expression of cubilin (show CUBN Antibodies) in humans.

  4. homozygous mutations affecting exons 1-4 of human AMN (show ABCD1 Antibodies) lead to megaloblastic anemia 1

  5. cubilin (show CUBN Antibodies) and amnionless are subunits of a novel cubilin (show CUBN Antibodies)/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 (show TRAF3 Antibodies) 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 (show TRAF3 Antibodies) is an essential component of the Cubn (show CUBN Antibodies) receptor complex

AMN Antigen Profile

Protein 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 anti-Amnionless (AMN) Antibodies

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

Protein level used designations for anti-Amnionless (AMN) Antibodies

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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