anti-ELOVL Fatty Acid Elongase 4 (ELOVL4) Antikörper

ELOVL4 encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Zusätzlich bieten wir Ihnen ELOVL4 Proteine (4) und viele weitere Produktgruppen zu diesem Protein an.

Alle Antikörper anzeigen Gen GeneID UniProt
ELOVL4 83603 Q9EQC4
ELOVL4 6785 Q9GZR5
ELOVL4 315851  
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Top anti-ELOVL4 Antikörper auf antikoerper-online.de

Showing 10 out of 64 products:

Katalog Nr. Reaktivität Wirt Konjugat Applikation Bilder Menge Anbieter Lieferzeit Preis Details
Human Kaninchen Unkonjugiert EIA, WB Western blot analysis of ELOVL4 Antibody (C-term) in 293 cell line lysates (35ug/lane). This demonstrates the ELOVL4 antibody detected the ELOVL4 protein (arrow). 0.4 mL Anmelden zum Anzeigen 6 bis 8 Tage
$390.50
Details
Human Kaninchen Unkonjugiert ELISA, WB Western blot analysis of extracts from HeLa cells, using ELOVL4 Antibody. The lane on the right is treated with the synthesized peptide. 100 μg Anmelden zum Anzeigen 2 bis 3 Tage
$302.50
Details
Human Kaninchen Unkonjugiert WB   0.1 mg Anmelden zum Anzeigen 11 bis 13 Tage
$468.05
Details
Human Kaninchen Unkonjugiert WB   0.1 mg Anmelden zum Anzeigen 6 bis 8 Tage
$390.50
Details
Human Kaninchen Unkonjugiert ELISA, WB 100 μL Anmelden zum Anzeigen 16 Days
$181.73
Details
Human Kaninchen Unkonjugiert WB ELOVL4 Antibody (C-term)  western blot analysis in 293 cell line lysates (35ug/lane).This demonstrates the ELOVL4 antibody detected the ELOVL4 protein (arrow). 400 μL Anmelden zum Anzeigen 10 bis 11 Tage
$324.50
Details
Human Kaninchen Unkonjugiert WB Western blot analysis of ELOVL4 expression in HY926 (A) whole cell lysates. 200 μL Anmelden zum Anzeigen 13 bis 14 Tage
$487.50
Details
Human Kaninchen Unkonjugiert IHC, WB 100 μL Anmelden zum Anzeigen 16 Days
$476.15
Details
Human Kaninchen Unkonjugiert IHC, WB 10 blots Anmelden zum Anzeigen 7 bis 9 Tage
$654.50
Details
Human Kaninchen Unkonjugiert ELISA, WB   200 μL Anmelden zum Anzeigen 7 bis 9 Tage
$793.83
Details

ELOVL4 Antikörper nach Reaktivität, Anwendung, Klonalität and Konjugat

Attribute Applikationen Wirt Klonalität Konjugat
Mouse (Murine) ,



Human ,
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Rat (Rattus) ,



Weitere Antikörper gegen ELOVL4 Interaktionspartner

Mouse (Murine) ELOVL Fatty Acid Elongase 4 (ELOVL4) Interaktionspartner

  1. Studies indicate that Knock-IN and Knock-OUT strains of ELOVL4 (STGD3) model development has been to unveil the causal connection between the genotype and early-onset progressive cone degeneration in humans.

  2. ELOVL4 enzymatic activity is governed by individual histidines in its active site and the endoplasmic reticulum microenvironment.

  3. To elucidate the role of VLC-PUFAs in photoreceptor terminals, we conditionally deleted Elovl4 in rod and cone photoreceptors of mice and measured inner retina function, synaptic connectivity, and ultrastructure of rod terminals with reduced VLC-PUFAs.

  4. expression and outer segment mislocalization of the disease-linked 5-base-pair deletion mutant ELOVL4 protein alters photoreceptor structure and function

  5. The mosaic deletion of rod-expressed ELOVL4 protein resulted in a 36 % lower amount of very long chain-PUFA in the retinal phosphatidylcholine (zeige SGMS2 Antikörper) (PC) fraction compared to retinas from wild-type mice.

  6. ELOVL4 was strongly expressed within the holocrine meibomian and sebaceous glands but no ELOVL4 was detected within the central meibomian duct.

  7. the presence of the mutant ELOVL4 does not affect the function of wild-type ELOVL4 in the fully developed 8- to 10-week-old retinas.

  8. Role of ELOVL4 and very long-chain polyunsaturated fatty acids in mouse models of Stargardt type 3 retinal degeneration.

  9. the critical role of Elovl4 for proper rod or cone photoreceptor function

  10. Epidermal expression of an Elovl4 transgene rescues neonatal lethality of homozygous Stargardt disease-3 mice.

Human ELOVL Fatty Acid Elongase 4 (ELOVL4) Interaktionspartner

  1. Swiss Family with Dominant Stargardt Disease Caused by a Recurrent Mutation in the ELOVL4 Gene

  2. In the control group, four different genetic variations were detected in ELOVL4, and five in PRPH2 (zeige PRPH2 Antikörper). STGD (zeige ABCA4 Antikörper) patients of different ethnicities may carry distinct ELOVL4 and PRPH2 (zeige PRPH2 Antikörper) sequence variants. We believe that the genetic variations identified in this study may be related to STGD (zeige ABCA4 Antikörper) etiopathogenesis.

  3. In patients with intrahepatic cholestasis of pregnancy, there was no elevation in ELOVL4 mRNA in maternal circulation compared with controls.

  4. Both ELOVL4- and PROM1-related maculopathies are characterized by progressive photoreceptor atrophy and central vision loss. Using advanced diagnostic imaging, early disease changes and disease progression can be characterized.

  5. different mutations in ELOVL4 can cause variable phenotypic neurological disorders (Review)

  6. Spinocerebellar ataxia was associated with a novel mutation in ELOVL4 in a large family pedigree.

  7. In this review, we summarize our current understanding of the disease-causing mutation and its potential role in STGD3 pathogenesis.

  8. We propose that transgenic expression of ELOVL4 in the liver will result in the biosynthesis of very long chain-PUFA that can be transported to target.

  9. ELOVL4 is identified as the causative gene for erythrokeratodermia variabilis and spinocerebellar ataxia in a French-Canadian family.

  10. A novel homozygous nonsense mutation in ELOVL4 cuases a neuro-ichthyotic disorder with variable expressivity.

ELOVL4 Antigen-Profil

Protein Überblick

This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration.

Genbezeichner und Symbole assoziert mit ELOVL4

  • elongation of very long chain fatty acids protein 4 (CpipJ_CPIJ002114) Antikörper
  • elongation of very long chain fatty acids protein 4 (CpipJ_CPIJ003687) Antikörper
  • elongation of very long chain fatty acids protein 4 (CpipJ_CPIJ011025) Antikörper
  • elongation of very long chain fatty acids protein 4 (CpipJ_CPIJ013819) Antikörper
  • ELOVL fatty acid elongase 4 (ELOVL4) Antikörper
  • elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 (elovl4) Antikörper
  • elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 (Elovl4) Antikörper
  • ELOVL fatty acid elongase 4 (Elovl4) Antikörper
  • ADMD Antikörper
  • CT118 Antikörper
  • elovl4 Antikörper
  • ISQMR Antikörper
  • MGC122553 Antikörper
  • STGD2 Antikörper
  • STGD3 Antikörper

Bezeichner auf Proteinebene für ELOVL4

elongation of very long chain fatty acids protein 4 , elongation of very long chain fatty acids (FEN1/Elo2, SUR4/Elo3, yeast)-like 4 , elongation of very long chain fatty acids family member protein 4 , ELOVL fatty acid elongase 4 , 3-keto acyl-CoA synthase Elovl4 , ELOVL FA elongase 4 , very-long-chain 3-oxoacyl-CoA synthase 4 , 3-keto acyl-CoA synthase ELOVL4 , Stargardt disease 3 (autosomal dominant) , cancer/testis antigen 118 , elongation of very long chain fatty acids-like 4 , elongation of very long chain fatty acids 4

GENE ID SPEZIES
6032855 Culex quinquefasciatus
6035294 Culex quinquefasciatus
6043662 Culex quinquefasciatus
6046870 Culex quinquefasciatus
421850 Gallus gallus
462842 Pan troglodytes
481894 Canis lupus familiaris
100124726 Xenopus (Silurana) tropicalis
100596130 Nomascus leucogenys
83603 Mus musculus
6785 Homo sapiens
315851 Rattus norvegicus
692070 Macaca mulatta
Ausgewählte Anbieter für anti-ELOVL4 (ELOVL4) Antikörper
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