epitope corresponding to amino acids 20-248 mapping near the N-terminus of Amnionless of mouse origin
Modification Notes
Megaloblastic anemia 1 (MGA1), also referred to as MGA1 Norwegian type or Imerslund-Grasbeck syndrome (I-GS), is a hereditary, recessive disorder caused by defects in the AMN gene. Patients suffering from MGA1 have a selective malabsorption of vitamin B12, causing impaired function of thymidine synthase which in turn interrupts DNA synthesis. Amnionless protein, encoded for by the AMN gene, is crucial for vitamin B12 absorption. It modulates a BMP (bone morphogenetic protein) signaling pathway and is therefore important for trunk mesoderm production during development. Amnionless is a membrane protein that interacts with cubulin and is primarily expressed in colon, kidney and small intestine. Shorter isoforms can also be detected in thymus, testis and peripheral blood leukocytes.
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of Amnionless of mouse, rat and, to a lesser extent, human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 20-248 mapping near the N-terminus of Amnionless of mouse origin
Tissue Specificity
epitope corresponding to amino acids 20-248 mapping near the N-terminus of Amnionless of mouse origin
Application
Application
Western blot analysis of Amnionless expression in mouse PBL whole cell lysate.
Application Notes
recommended for detection of Amnionless of mouse, rat and, to a lesser extent, human origin by WB, IP, IF and ELISA:
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.