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Mouse Monoclonal ApoL1 antibody [1D4] (STJ97840)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, ELISA
Recommended dilution: WB 1:500-1:2000; ELISA 1:10000
Recommended protocols: check protocols
Click or hover above images to see image description for ApoL1 Monoclonal Antibody.
Check alternative names for the antibodyExpand
APOL1 antibody, APOL antibody,|APO L antibody|Apo-L antibody|ApoL antibody|APOL I antibody|ApoL-I antibody|APOL1 antibody|APOL1_HUMAN antibody|APOLI antibody|Apolipoprotein L antibody|Apolipoprotein L I antibody|Apolipoprotein L-I antibody|Apolipoprotein L1 antibody|FSGS4 antibody|Anti-Apolipoprotein L 1 antibody [EPR2907(2)] (ab108315)
SCBT cat No: sc-390440|sc-30090|sc-18759|
ApoL1 Monoclonal Antibody
|Catalogue No.|| |
ApoL1 Monoclonal Antibody detects endogenous levels of ApoL1 protein.
Purified recombinant fragment of ApoL1 expressed in E Coli
|Recommended dilution|| |
WB 1:500-1:2000; ELISA 1:10000
ApoL1 Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.
ApoL1 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Apolipoprotein L1 antibody, Apolipoprotein L antibody, Apo-L antibody, ApoL antibody, Apolipoprotein L-I antibody, ApoL-I antibody
|Protein names|| |
Apolipoprotein L1 , Apolipoprotein L , Apo-L , ApoL , Apolipoprotein L-I , ApoL-I
|Protein function|| |
May play a role in lipid exchange and transport throughout the body. May participate in reverse cholesterol transport from peripheral cells to the liver.
|Protein tissue specificity|| |
Plasma. Found on APOA-I-containing high density lipoprotein (HDL3). Expressed in pancreas, lung, prostate, liver, placenta and spleen.
|Involvement in disease|| |
Focal segmental glomerulosclerosis 4 (FSGS4) [MIM:612551]: A renal pathology defined by the presence of segmental sclerosis in glomeruli and resulting in proteinuria, reduced glomerular filtration rate and progressive decline in renal function. Renal insufficiency often progresses to end-stage renal disease, a highly morbid state requiring either dialysis therapy or kidney transplantation. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the apolipoprotein L family.
|Protein post-translational modifications|| |
Phosphorylated by FAM20C in the extracellular medium.
|Protein cellular localization|| |
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St John’s Laboratory Ltd.
|Product type|| |
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