ApoL2 rabbit polyclonal, anti-human, mouse, rat

Backgroud: 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. [provided by RefSeq, Jul 2008],function:May affect the movement of lipids in the cytoplasm or allow the binding of lipids to organelles.,similarity:Belongs to the apolipoprotein L family.,tissue specificity:Widely expressed; the highest levels are found in lung, thymus, pancreas, placenta, adult brain and prostate; also detected in spleen, liver, kidney, colon, small intestine, uterus, spinal cord, adrenal gland, salivary gland, trachea, mammary gland, skeletal muscle, testis and fetal brain and liver.,

Synonyms: APOL2, Apolipoprotein L2, Apolipoprotein L-II, ApoL-II

Gene Name: APOL2

Gene ID: 23780

SwissProt ID: Q9BQE5

Purification: Affinity purification

Storage: Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.