Apolipoprotein L, 1 (APOL1) ELISA Kits

APOL1 encodes a secreted high density lipoprotein which binds to apolipoprotein A-I. Zusätzlich bieten wir Ihnen APOL1 Antikörper (140) und APOL1 Proteine (5) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
APOL1 8542 O14791
APOL1    
APOL1    
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Top APOL1 ELISA Kits auf antikoerper-online.de

Showing 10 out of 34 products:

Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Lieferzeit Preis Details
Human 0.51 ng/mL 1.25 ng/mL - 80 ng/mL 96 Tests 13 bis 16 Tage
$736.84
Details
Ratte 7.1 pg/mL 15.6 pg/mL - 1000 pg/mL 96 Tests 13 bis 16 Tage
$800.00
Details
Kaninchen 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 bis 18 Tage
$707.14
Details
Meerschweinchen 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 bis 18 Tage
$707.14
Details
Maus 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 bis 18 Tage
$707.14
Details
Affe 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 bis 18 Tage
$707.14
Details
Hund 0.1 ng/mL 2.5-50 ng/mL   96 Tests 15 bis 18 Tage
$707.14
Details
Schwein
  96 Tests 15 bis 18 Tage
$707.14
Details
Ziege
  96 Tests 15 bis 18 Tage
$707.14
Details
Huhn
  96 Tests 15 bis 18 Tage
$707.14
Details

Am meisten referenzierte APOL1 ELISA Kits

  1. Human APOL1 ELISA Kit für Sandwich ELISA - ABIN419395 : Van Vinh Chau, Buu Chau, Desquesnes, Herder, Phu Huong Lan, Campbell, Van Cuong, Yimming, Chalermwong, Jittapalapong, Ramon Franco, Tri Tue, Rabaa, Carrique-Mas, Pham Thi Thanh, Tran Vu Thieu, Berto et al.: A Clinical and Epidemiological Investigation of the First Reported Human Infection With the Zoonotic Parasite Trypanosoma evansi in Southeast Asia. ... in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2016 (PubMed)

Weitere ELISA Kits für APOL1 Interaktionspartner

Human Apolipoprotein L, 1 (APOL1) Interaktionspartner

  1. APOL1 high-risk status is associated with CVD events in community-dwelling Black adults without diabetes mellitus.

  2. ApoL1 variants regulate monocyte differentiation into macrophages and eicosanoid metabolism via enhanced COX-2 expression.

  3. Among blacks without baseline CVD, the APOL1 high-risk variants may be associated with increased risk for incident heart failure but not subclinical CVD or incident clinical atherosclerotic CVD.

  4. Donor APOL1 high-risk genotypes are associated with inferior graft survival and de novo collapsing focal segmental glomerulosclerosis with high proteinuria after kidney transplantation.

  5. Individual genome-wide association studies and meta-analysis results of 2650 end-stage renal disease (ESRD) cases and 1656 controls African American patients did not detect significant genome-wide associations with ESRD beyond APOL1. Similarly, no single nucleotide polymorphism showed significant genome-wide evidence of an interaction with APOL1 risk variants. [meta-analysis]

  6. Fetal APOL1 high-risk genotype increases the risk for preeclampsia, likely by adversely affecting placental function.

  7. These studies establish APOL1 as a bona fide LD-associated protein, and reveal that recruitment of risk variant APOL1 to LDs reduces cell toxicity, autophagic flux, and cell death.

  8. APOL1 genotype may not be sufficient to explain discrepancies in postdonation kidney function between caucasian donors and low-risk APOL1 genotype living kidney donors of African ancestry.

  9. APOL1 risk variants contribute to podocyte injury through enhanced endoplasmic reticulum stress. The study provides insight into new mechanisms involved in APOL1 risk variants-induced podocyte damage, and highlights some new therapeutic targets for APOL1-associated nephropathy.

  10. Apolipoprotein L1 risk variants are present in black South Africans with similar frequencies between chronic kidney disease patients, first-degree relatives, and healthy controls.

  11. Plasma concentrations of TNFR1, TNFR2, and KIM1 are independently associated with renal outcome and improve discrimination or reclassification of African ancestry individuals with a high-risk APOL1 genotype and preserve renal function.

  12. APOL1 risk variants did not associate with subclinical markers of atherosclerosis or left ventricular hypertrophy in middle-aged black adults with preserved kidney function.

  13. Review of the role of APOL1 in kidney disease in children and young adults of African ancestry. APOL1 explains almost 70% of the excess risk of kidney disease in those of African descent, and is common in children with glomerular disease.

  14. Association of chronic kidney disease with APOL1 risk alleles was not identified in Aboriginal people in remote areas of Australia.

  15. APOL1 Risk Variant is associated with focal segmental glomerulosclerosis.

  16. APOL1, alpha-thalassemia, and BCL11A variants as a genetic risk profile for progression of chronic kidney disease in sickle cell anemia.

  17. Among blacks with established moderate CKD, the APOL1 high-risk variants are associated with greater risk of incident proteinuria. After proteinuria onset, kidney function declines more rapidly but does not differ by APOL1 risk status.

  18. In individuals at risk for nondiabetic kidney disease based on African ancestry, the majority of that risk can be explained by two variants in the APOL1 gene.

  19. Considering APOL1 evolution also may help us understand how APOL1 risk variants cause kidney disease in modern humans.

  20. APOL1 variants are associated with HIV-associated nephropathy(HIVAN), a podocyte disease,but not with HIV-immune complex disease, primarily a disease of the mesangium.

Zebrafish Apolipoprotein L, 1 (APOL1) Interaktionspartner

  1. zApoL1 is essential for proper blood filtration in the zebrafish glomerulus and that zApoL1 affects the expression of nephrin

APOL1 Antigen-Profil

Beschreibung des Gens

This gene encodes a secreted high density lipoprotein which binds to apolipoprotein A-I. Apolipoprotein A-I is a relatively abundant plasma protein and is the major apoprotein of HDL. It is involved in the formation of most cholesteryl esters in plasma and also promotes efflux of cholesterol from cells. 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.

Genbezeichner und Symbole assoziert mit Apolipoprotein L, 1 (APOL1) ELISA Kits

  • apolipoprotein L1 (APOL1) Antikörper
  • apolipoprotein L, 1 (apol1) Antikörper
  • APO-L Antikörper
  • APOL Antikörper
  • APOL-I Antikörper
  • FSGS4 Antikörper
  • si:rp71-1g18.12 Antikörper
  • wu:fa95b12 Antikörper
  • wu:fc30h04 Antikörper

Bezeichner auf Proteinebene für Apolipoprotein L, 1 (APOL1) ELISA Kits

apolipoprotein L1

GENE ID SPEZIES
8542 Homo sapiens
560340 Danio rerio
Ausgewählte Anbieter für APOL1 (APOL1) ELISA Kits
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