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Supplier : Arigo Biolaboratories
|Production type||ELISA Kits|
|Specificity||No significant cross-reactivity or interference with Human ApoB, ApoC1, ApoC2, ApoC3, ApoD, ApoE, ApoE3, ApoER2, ApoH, ApoJ, ApoM|
|Conjugation Note||Substrate: TMB and read at 450 nm|
|Detection Range||3.125-200 ng/ml|
|Sample Type||Serum, Plasma, Cell culture supernatants|
|Sample Volume||100 ul|
|Full Name||apolipoprotein A-I|
|Alternate Names||Check alternative names for the Human apoA1 ELISA Kit Expand
Apo-AI Elisa kits|ApoA I Elisa kits|ApoA-I Elisa kits|APOA1 Elisa kits|APOA1_HUMAN Elisa kits|Apolipoprotein A-I(1-242) Elisa kits|Apolipoprotein A1 Elisa kits|Apolipoprotein AI Elisa kits|Brp14 Elisa kits|Ltw1 Elisa kits|Lvtw1 Elisa kits|Sep1 Elisa kits|Sep2 Elisa kits
|Assay Time||4 hours|
|Storage instruction||Store the kit at 2-8°C. Keep microplate wells sealed in a dry bag with desiccants. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components or simply ask Antibodyplus for ELISA troublesooting.|
|Note||Antibodyplus and Arigo provide the most validated ELISA kits for researchers. For laboratory research only, not for drug, diagnostic or other use.|
|User’s manual of Human apoA1 ELISA Kit||Download|
|Cat No.|| |
|Conjugation note|| |
Substrate: TMB and read at 450 nm
|Detection range|| |
|Sample type|| |
Serum, Plasma, Cell culture supernatants
|Sample Volume|| |
|Target name|| |
|Assay time|| |
|Store at|| |
4 Celcius degree
|Storage instruction|| |
Store the kit at 2-8 Celcius degree. Keep microplate wells sealed in a dry bag with desiccants. Do not expose test reagents to heat, sun or strong light during storage and usage. Please refer to the product user manual for detail temperatures of the components.
This gene encodes apolipoprotein A-I, which is the major protein component of high density lipoprotein (HDL) in plasma. The protein promotes cholesterol efflux from tissues to the liver for excretion, and it is a cofactor for lecithin cholesterolacyltransferase (LCAT) which is responsible for the formation of most plasma cholesteryl esters. This gene is closely linked with two other apolipoprotein genes on chromosome 11. Defects in this gene are associated with HDL deficiencies, including Tangier disease, and with systemic non-neuropathic amyloidosis. [provided by RefSeq, Jul 2008]
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