AMN
-
Official Full Name
amnionless homolog (mouse)
-
Overview
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. -
Synonyms
AMN; amnionless homolog (mouse); protein amnionless; visceral endoderm-specific type 1 transmembrane protein; PRO1028;
- Recombinant Proteins
- Protein Pre-coupled Magnetic Beads
- Chicken
- Human
- Mouse
- Rat
- E.coli
- HEK293
- HEK293T
- Mammalian Cell
- Mammalian cells
- His
- His (Fc)
- Avi
- Myc
- DDK
- Myc|DDK
- N
Species | Cat.# | Product name | Source (Host) | Tag | Protein Length | Price |
---|---|---|---|---|---|---|
Human | AMN-777H | Active Recombinant Human AMN Protein, His-tagged | Mammalian cells | His | Val20-Ala358 | |
Human | AMN-768H | Recombinant Human AMN | Mammalian Cell | His | ||
Human | AMN-7084H | Recombinant Human AMN, His-tagged | E.coli | His | 20-357aa | |
Human | AMN-1987H | Recombinant Human AMN Protein, MYC/DDK-tagged | HEK293 | Myc/DDK | ||
Human | AMN-2462H-B | Recombinant Human AMN Protein Pre-coupled Magnetic Beads | HEK293 | |||
Human | AMN-2462H | Recombinant Human AMN Protein, His (Fc)-Avi-tagged | HEK293 | His (Fc)-Avi | ||
Mouse | Amn-1612M | Recombinant Mouse Amn Protein, Myc/DDK-tagged | HEK293T | Myc/DDK | ||
Rat | Amn-136R | Recombinant Rat Amn Protein, His-tagged | E.coli | N-His | Ala20-Glu268 | |
Chicken | AMN-4907C | Recombinant Chicken AMN | Mammalian Cell | His |
- Involved Pathway
- Protein Function
- Interacting Protein
- AMN Related Articles
- AMN Related Research Area
AMN involved in several pathways and played different roles in them. We selected most pathways AMN participated on our site, such as Cobalamin (Cbl, vitamin B12) transport and metabolism, Defective AMN causes hereditary megaloblastic anemia 1, Defective CUBN causes hereditary megaloblastic anemia 1, which may be useful for your reference. Also, other proteins which involved in the same pathway with AMN were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.
Pathway Name | Pathway Related Protein |
---|---|
Cobalamin (Cbl, vitamin B12) transport and metabolism | ELA2L;MMADHC;LOC100686744;TCN1;AMN;CTRC;CD320;CBLC-1;ELA2 |
Defective AMN causes hereditary megaloblastic anemia 1 | |
Defective CUBN causes hereditary megaloblastic anemia 1 | |
Defects in cobalamin (B12) metabolism | AMN;MTRR;MMADHC;MMAA |
Defects in vitamin and cofactor metabolism | AMN;MMAA;MTRR;MMADHC |
Disease | JAG2;PSIP1;NUP35;PSTPIP2;RNF43;OS9;DERL2;CHMP4B;gag |
Diseases of metabolism | GYG1;MTRR;MMAA;MMADHC;SFTPC;EPM2A;CYP11A1;GYG2;CCDC59 |
HDL-mediated lipid transport | CETP;BMP1A;Alb;APOA1B;APOC2;ABCA1;AMN |
AMN has several biochemical functions, for example, receptor binding. Some of the functions are cooperated with other proteins, some of the functions could acted by AMN itself. We selected most functions AMN had, and list some proteins which have the same functions with AMN. You can find most of the proteins on our site.
Function | Related Protein |
---|---|
receptor binding | INHA;NPFF;PLAUR;BMP3;TMED1;FGF10B;NPPC;SRPX2;FRK |
AMN has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with AMN here. Most of them are supplied by our site. Hope this information will be useful for your research of AMN.
- Q&As
- Reviews
Q&As (0)
Ask a questionAsk a Question for All AMN Products
Required fields are marked with *
My Review for All AMN Products
Required fields are marked with *