Apolipoprotein L (APOL1) Antibody

383.5€ (100 µl)
Este producto es parte de APOL1 - Apolipoprotein L1
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383.5€ (100 µl)

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935106861
info@markelab.com
name
Apolipoprotein L (APOL1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx015721
tested applications
ELISA, WB

Descripción del producto

APOL1 (apolipoprotein L, 1), also known as APOL, APO-L, APOL-I.Entrez Protein NP_001130012.It is a 395aa secreted high density lipoprotein which binds to apolipoprotein A-I.And is involved in the formation of most cholesteryl esters in plasma and also promotes efflux of cholesterol from cells.The apolipoprotein L gene family encodes six highly homologous proteins designated apoL-I to -VI.This apolipoprotein L family member may play a role in lipid exchange and transport throughout the body, as well as in reverse cholesterol transport from peripheral cells to the liver.Several different transcript variants encoding different isoforms have been found for this gene.

Documents del producto

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Especificaciones del producto

OMIM603743
AliasAPOL1, APO-L, APOL, APOL-I, FSGS4, apolipoprotein L1, APO L1
AvailabilityShipped within 5-10 working days.
BackgroundAntibody anti-APOL1
BufferAscitic fluid containing 0.03% sodium azide.
CategoryPrimary Antibodies
ClonalityMonoclonal
ConjugationUnconjugated
Dry IceNo
FormLiquid
Gene ID8542
HostMouse
Immunogen TargetApolipoprotein L (APOL1)
IsotypeIgG1
NameApolipoprotein L (APOL1) Antibody
NoteConcentration: Not determined. -
Price383.5
ProviderAbbexa
PurificationUnpurified ascites.
ReactivityHuman
Recommended DilutionELISA: 1/10000, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Referenceabx015721
Size 1100 µl
StatusRUO
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Tested ApplicationsELISA, WB
UniProt IDO14791

Descripcion del producto en español

Background en español

Apolipoprotein L1 (APOL1) is a member of the Apolipoprotein L gene family and plays a critical role in lipid transport and innate immunity. APOL1 is primarily expressed in the liver, kidney, and vascular endothelium and is known for its ability to bind high-density lipoprotein (HDL) particles, contributing to lipid transport and cholesterol metabolism. A particularly vital function of APOL1 lies in its role in innate immunity, as it helps protect against trypanosome infections. APOL1 can lyse trypanosomes such as Trypanosoma brucei, which cause African sleeping sickness, by disrupting their cellular membranes. Genetic variations, specifically the G1 and G2 risk alleles, have been associated with increased susceptibility to kidney diseases, such as focal segmental glomerulosclerosis (FSGS) and HIV-associated nephropathy (HIVAN), particularly in people of African descent. These alleles enhance APOL1-mediated trypanosome resistance but lead to cytotoxic effects in kidney cells under specific stress conditions. APOL1’s dual role as both a defender against pathogens and a contributor to renal disease makes it a subject of intensive research. Targeting APOL1 signaling pathways may provide therapeutic options for managing kidney diseases and understanding its broader impact on lipid metabolism and immune responses.

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