Fatty Acid 2-Hydroxylase (FA2H) Kits ELISA

FA2H encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. De plus, nous expédions FA2H Anticorps (48) et FA2H Protéines (4) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
FA2H 79152 Q7L5A8
FA2H 307855 Q2LAM0
FA2H 338521 Q5MPP0
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Top FA2H Kits ELISA sur anticorps-enligne.fr

Showing 3 out of 6 products:

Catalogue No. Reactivité Sensibilité Gamme Images Quantité Fournisseur Livraison Prix Détails
Souris < 46.9 pg/mL 78 pg/mL - 5000 pg/mL   96 Tests Connectez-vous pour afficher 11 to 18 Days
$810.17
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Humain < 0.188 ng/mL 0.313 ng/mL - 20 ng/mL   96 Tests Connectez-vous pour afficher 11 to 18 Days
$810.17
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Rat < 0.094 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests Connectez-vous pour afficher 11 to 18 Days
$810.17
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Plus Kits ELISA pour FA2H partenaires d'interaction

Human Fatty Acid 2-Hydroxylase (FA2H) interaction partners

  1. Novel variant c.130C>T (p.Pro44Ser) in homozygous status in exon 1 of the FA2H gene is described in a Czech patient with SPG35.

  2. PGRMC1 may regulate FA2H activity, possibly through its heme chaperone activity.

  3. Novel mutations in FA2H in Arab patients with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis were identified.

  4. Three novel mutations in Chinese patients significantly reduce FA2H enzyme activity leading to hereditary spastic paraplegia.

  5. Induced levels of PPARalpha may be involved in the Delta(9)-THC up-regulation of FA2H in MDA-MB-231 cells.

  6. One heterozygous deletion within 16q22.3-q23.1 including FA2H was observed in two siblings who share symptoms of autism and severe cognitive impairment, axial T2-FLAIR weighted MRI posterior periventricular white matter lesions.

  7. Identification of a novel triple heterozygous mutations in FA2H gene (c.968C>A; c.976G>A; c.688G>A) in a Chinese family with Hereditary Spastic Paraplegia Type 35.

  8. FA2H is a novel (9)-THC-regulated gene, and that (9)-THC induces differentiation signal(s) in poorly differentiated MDA-MB-231 cells.

  9. we report a novel mutation in FA2H gene in two sibs presenting with adult onset complicated spastic paraparesis and thin corpus callosum

  10. This study did not find any mutations in the FA2H gene in patients with neurodegeneration with brain iron accumulation.

  11. a novel homozygous c.270+3A>T mutation altered FA2H function led to a severe phenotype, with clinical features overlapping those in three FA2H-associated disorders

  12. The 2-hydroxylated sphingomyelin (SM) profiles were characterized in blood and fibroblasts from patients harboring a deleterious FA2H mutation.

  13. Mutations in FA2H are associated with hereditary spastic paraplegia.

  14. the human FA2H gene encodes a fatty acid 2-hydroxylase involved in the formation of myelin 2-hydroxy galactosylceramides and -sulfatides

  15. late differentiation-linked increases in FA2H expression are essential for epidermal permeability barrier homeostasis.

  16. Mutations in FA2H are associated with leukodystrophy with spastic paraparesis and dystonia.

Mouse (Murine) Fatty Acid 2-Hydroxylase (FA2H) interaction partners

  1. the importance of the sebaceous glands and a role of specific sebaceous gland or sebum lipids, synthesized by FA2H, in the hair follicle homeostasis

  2. This study provided the first evidence that FA2H has an important function outside of oligodendrocytes in the Central nervous system.

  3. Our study showed that the additional deletion of Fa2h does not obviously affect the phenotype of Cgt-/- mice. This suggests that HFA-GlcCer and HFA-sphingomyelin do not functionally compensate the loss of HFA-GalCer in Cgt-/- mice.

  4. Fndings document the novel role of FA2H in adipocyte lipogenesis possibly by modulation of raft fluidity and level of GLUT4.

  5. FA2H is the enzyme responsible for the formation of alpha-hydroxylated ceramide in oligodendrocytes of the mammalian brain.

  6. FA2H is the major fatty acid 2-hydroxylase in brain, and 2-hydroxylation of free fatty acids is the first step in the synthesis of 2-hydroxy galactolipids

FA2H profil antigène

Antigen Summary

This gene encodes a protein that catalyzes the synthesis of 2-hydroxysphingolipids, a subset of sphingolipids that contain 2-hydroxy fatty acids. Sphingolipids play roles in many cellular processes and their structural diversity arises from modification of the hydrophobic ceramide moiety, such as by 2-hydroxylation of the N-acyl chain, and the existence of many different head groups. Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia.

Gene names and symbols associated with FA2H

  • fatty acid 2-hydroxylase (FA2H) anticorps
  • fatty acid 2-hydroxylase (Fa2h) anticorps
  • fatty acid 2-hydroxylase L homeolog (fa2h.L) anticorps
  • fatty acid 2-hydroxylase (fa2h) anticorps
  • fatty acid 2-hydroxylase (Tsp_11648) anticorps
  • fatty acid hydroxylase (Ilyop_0703) anticorps
  • fatty acid hydroxylase (Celly_1453) anticorps
  • fatty acid hydroxylase (Weevi_1515) anticorps
  • fatty acid hydroxylase (Fluta_1455) anticorps
  • fatty acid hydroxylase (Mesop_3301) anticorps
  • cb1044 anticorps
  • FAAH anticorps
  • FAH1 anticorps
  • Faxdc1 anticorps
  • G630055L08Rik anticorps
  • MGC85470 anticorps
  • MGC97767 anticorps
  • RGD1310347 anticorps
  • SCS7 anticorps
  • SPG35 anticorps
  • Wdr59 anticorps
  • zgc:153777 anticorps

Protein level used designations for FA2H

fatty acid alpha-hydroxylase , fatty acid hydroxylase domain containing 1 , spastic paraplegia 35 (autosomal recessive) , WD repeat domain 59 , fatty acid 2-hydroxylase , fatty acid 2-hydroxylase-like , fatty acid hydroxylase

GENE ID SPECIES
79152 Homo sapiens
307855 Rattus norvegicus
338521 Mus musculus
398669 Xenopus laevis
415687 Gallus gallus
454243 Pan troglodytes
516891 Bos taurus
595069 Xenopus (Silurana) tropicalis
610417 Canis lupus familiaris
792257 Danio rerio
10903185 Trichinella spiralis
9868204 Ilyobacter polytropus DSM 2926
10263467 Cellulophaga lytica DSM 7489
10282765 Weeksella virosa DSM 16922
10396804 Fluviicola taffensis DSM 16823
10827138 Mesorhizobium opportunistum WSM2075
100734359 Cavia porcellus
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