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APOL2 is a member of the apolipoprotein L gene family.
Showing 10 out of 59 products:
Human Polyclonal Apolipoprotein L 2 Primary Antibody for ELISA, WB - ABIN449572
Mimmack, Ryan, Baba, Navarro-Ruiz, Iritani, Faull, McKenna, Jones, Arai, Starkey, Emson, Bahn: Gene expression analysis in schizophrenia: reproducible up-regulation of several members of the apolipoprotein L family located in a high-susceptibility locus for schizophrenia on chromosome 22. in Proceedings of the National Academy of Sciences of the United States of America 2002
Human Polyclonal Apolipoprotein L 2 Primary Antibody for ICC, IF - ABIN4281234
Galindo-Moreno, Iurlaro, El Mjiyad, Díez-Pérez, Gabaldón, Muñoz-Pinedo: Apolipoprotein L2 contains a BH3-like domain but it does not behave as a BH3-only protein. in Cell death & disease 2014
Apolipoprotein L2 contains a BH3-like domain but it does not behave as a BH3-only (show BBC3 Antibodies) protein.
Results reveal a novel function for ApoL2 in conferring anti-apoptotic ability of human bronchial epithelium to the cytotoxic effects of IFN-gamma (show IFNG Antibodies), in maintaining airway epithelial layer integrity.
An association of APOL1 (show APOL1 Antibodies), 2 and 4 with schizophrenia was establised.
APOL2 has been found only in humans and African green monkeys
This gene is a member of the apolipoprotein L gene family. The encoded protein is found in the cytoplasm, where it may affect the movement of lipids or allow the binding of lipids to organelles. Two transcript variants encoding the same protein have been found for this gene.
, apolipoprotein L-II
, apolipoprotein L, 2
, apolipoprotein L 8