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anti-ELOVL Fatty Acid Elongase 4 (ELOVL4) Antibodies

ELOVL4 encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Additionally we are shipping ELOVL4 Proteins (4) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
ELOVL4 83603 Q9EQC4
ELOVL4 6785 Q9GZR5
ELOVL4 315851  
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Top anti-ELOVL4 Antibodies at antibodies-online.com

Showing 10 out of 57 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated 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 Log in to see 6 to 8 Days
$390.50
Details
Human Rabbit Un-conjugated WB   0.1 mg Log in to see 6 to 8 Days
$390.50
Details
Human Rabbit Un-conjugated EIA, WB   0.1 mg Log in to see 6 to 8 Days
$456.50
Details
Human Rabbit Un-conjugated EIA, WB   0.25 mg Log in to see 10 to 12 Days
$485.10
Details
Human Rabbit Un-conjugated 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 Log in to see 2 to 3 Days
$302.50
Details
Human Rabbit Un-conjugated 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 Log in to see 10 to 11 Days
$324.50
Details
Human Rabbit Un-conjugated EIA, WB   0.1 mg Log in to see 6 to 8 Days
$456.50
Details
Human Rabbit Un-conjugated ELISA, WB 100 μL Log in to see 8 to 10 Days
$478.50
Details
Human Rabbit Un-conjugated WB Western blot analysis of ELOVL4 expression in HY926 (A) whole cell lysates. 200 μL Log in to see 9 Days
$487.50
Details
Human Rabbit Un-conjugated WB 100 μL Log in to see 14 Days
$527.15
Details

ELOVL4 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality Conjugate
Mouse (Murine) ,


Human ,
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, , , , ,
Rat (Rattus) ,


Top referenced anti-ELOVL4 Antibodies

  1. Human Polyclonal ELOVL4 Primary Antibody for EIA, WB - ABIN952069 : Kasperaviciūte, Catarino, Heinzen, Depondt, Cavalleri, Caboclo, Tate, Jamnadas-Khoda, Chinthapalli, Clayton, Shianna, Radtke, Mikati, Gallentine, Husain, Alhusaini, Leppert, Middleton, Gibson, Johnson, Matthews, Hosford, Heuser, Amos, Ortega, Zumsteg, Wie: Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. in Brain : a journal of neurology 2010 (PubMed)
    Show all 4 references for ABIN952069

  2. Human Polyclonal ELOVL4 Primary Antibody for EIA, WB - ABIN492960 : Edwards, Donoso, Ritter: A novel gene for autosomal dominant Stargardt-like macular dystrophy with homology to the SUR4 protein family. in Investigative ophthalmology & visual science 2001 (PubMed)

  3. Human Polyclonal ELOVL4 Primary Antibody for WB - ABIN265287 : Kobayashi, Zadravec, Jacobsson: ELOVL2 overexpression enhances triacylglycerol synthesis in 3T3-L1 and F442A cells. in FEBS letters 2007 (PubMed)

More Antibodies against ELOVL4 Interaction Partners

Mouse (Murine) ELOVL Fatty Acid Elongase 4 (ELOVL4) interaction partners

  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 (show SGMS2 Antibodies) (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) interaction partners

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

  2. 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.

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

  4. Spinocerebellar ataxia (show USP14 Antibodies) was associated with a novel mutation in ELOVL4 in a large family pedigree.

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

  6. 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.

  7. ELOVL4 is identified as the causative gene for erythrokeratodermia variabilis and spinocerebellar ataxia (show USP14 Antibodies) in a French-Canadian family.

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

  9. Coexpression of different forms of wild-type and mutant ELOVL4 revealed a large dominant-negative effect of mutant protein on ELOVL4 localization and enzymatic activity, resulting in reduced VLC-PUFA synthesis.

  10. 5 single nucleotide polymorphisms (SNPs: rs3812153, rs7764439, rs390659, rs434102 and c:929G>A) were detected in ELOVL4.

ELOVL4 Antigen Profile

Protein Summary

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.

Gene names and symbols associated with ELOVL4

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

Protein level used designations for 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 SPECIES
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
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