Product Name: ABP1 Antibody
Species Reactivity: Human
Tested Applications: ELISA, IHC, WB
Applications: ABP1 antibody can be used for detection of ABP1 by ELISA at 1:312500. ABP1 antibody can be used for detection of ABP1 by western blot at 1.0 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 – 100,000.
User Note: Optimal dilutions for each application to be determined by the researcher.
Predicted Molecular Weight: 83 kDa
Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human ABP1.
Host Species: Rabbit
Purification: Antibody is purified by peptide affinity chromatography method.
Physical State: Lyophilized
CAS NO.: 141117-12-6
Product: Celgosivir (hydrochloride)
Buffer: Antibody is lyophilized in PBS buffer with 2% sucrose. Add 50 μL of distilled water. Final antibody concentration is 1 mg/mL.
Concentration: 1 mg/ml
Storage Conditions: For short periods of storage (days) store at 4˚C. For longer periods of storage, store ABP1 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: ABP1, ABP, AOC1, DAO, DAO1, KAO, ABP1
Accession NO.: NP_001082
Protein Ino: 73486661
Official Symbol: AOC1
Geneid: 26
Background: ABP1 is a membrane glycoprotein that is expressed in many epithelium-rich and/or hematopoietic tissues and oxidatively deaminates putrescine and histamine. The protein may play a role in controlling the level of histamine and/or putrescine in these tissues. It also binds to and is inhibited by amiloride, a diuretic that acts by closing epithelial sodium ion channels.This gene encodes a membrane glycoprotein that is expressed in many epithelium-rich and/or hematopoietic tissues and oxidatively deaminates putrescine and histamine. The protein may play a role in controlling the level of histamine and/or putrescine in these tissues. It also binds to and is inhibited by amiloride, a diuretic that acts by closing epithelial sodium ion channels.
PubMed ID:http://aac.asm.org/content/51/12/4486.abstract
