|Application ||WB, IHC-P, IF|
|Predicted||Human, Mouse, Rat|
|Calculated MW||84622 Da|
|Dilution||IF, IHC-P (1:100), WB|
|Other Names||AOC3, Copper amine oxidase, HPAO, Membrane primary amine oxidase, SSAO, VAP-1, VAP1, Vascular adhesion protein 1|
|Target/Specificity||Human AOC3 / VAP-1|
|Reconstitution & Storage||Affinity purified|
|Precautions||Anti-AOC3 / VAP-1 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Cell adhesion protein that participates in lymphocyte extravasation and recirculation by mediating the binding of lymphocytes to peripheral lymph node vascular endothelial cells in an L-selectin-independent fashion. Has semicarbazide-sensitive (SSAO) monoamine oxidase activity. May play a role in adipogenesis.|
|Cellular Location||Cell membrane; Single-pass type II membrane protein|
|Tissue Location||Strongly expressed on the high endothelial venules of peripheral lymph nodes and on hepatic endothelia. Also highly expressed in appendix, lung and small intestine. Expressed also in adipose tissue, in bone marrow, colon, heart, kidney, ovary, pancreas, placenta, prostate, skeletal muscle, spleen and testis. Isoform 2 seems to be the predominant transcript in fetal kidneys, fetal cartilage and fetal tonsils. The highest relative expression of isoform 2 occurs in skeletal muscle, heart, pancreas, kidney, and lung.|
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