Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase 3 (PLOD3) Kits ELISA

The protein encoded by PLOD3 is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. De plus, nous expédions PLOD3 Anticorps (55) et PLOD3 Protéines (5) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
Anti-Souris PLOD3 PLOD3 26433 Q9R0E1
Anti-Rat PLOD3 PLOD3 288583 Q5U367
PLOD3 8985 O60568
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Catalogue No. Reactivité Sensibilité Gamme Images Quantité Fournisseur Livraison Prix Détails
Humain 0.113 ng/mL 0.31 ng/mL - 20 ng/mL 96 Tests Connectez-vous pour afficher 13 to 16 Days

Plus Kits ELISA pour PLOD3 partenaires d'interaction

Zebrafish Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase 3 (PLOD3) interaction partners

  1. LH3 directs target-selective motor axon regeneration.

  2. Together these data suggest that Lh3-Collagen18A1 dependent ECM modifications regulate the transition of trunk neural crest cells from a non-segmental sheet like migration mode to a segmental stream migration mode

  3. diwanka (lh3) acts through myotomal type XVIII collagen, a ligand for neural-receptor protein tyrosine phosphatases that guide motor axons

Mouse (Murine) Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase 3 (PLOD3) interaction partners

  1. Data indicate that lysyl hydroxylase 3 is essential for the glucosyltion of mannan-binding lectin MBL-A.

  2. LH3 is an important regulator of adiponectin biosynthesis, secretion and activity.

  3. LH3-mediated glucosylation occurs at the specific molecular loci in the type I collagen molecule and plays critical roles in controlling collagen cross-linking, fibrillogenesis, and mineralization.

  4. the major function of LH3 in osteoblasts is to glucosylate galactosylhydroxylysine residues in type I collagen and that an impairment of this LH3 function significantly affects type I collagen fibrillogenesis.

  5. results demonstrate that LH3 is indispensable for biosynthesis of type IV collagen and for basement membrane stability during early development and that loss of LH3's functions leads to embryonic lethality

  6. LH3 is present and active in the extracellular space

  7. LH3 has lysyl hydroxylase and galactosylhydroxylysyl glucosyltransferase T activities in vivo, and is essential for the formation of the basement membrane

  8. Results report an important role for lysyl hydroxylase 3 in the organization of the extracellular matrix (ECM) and cytoskeleton.

Human Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase 3 (PLOD3) interaction partners

  1. VIPAR, with its partner proteins, regulate sorting of lysyl hydroxylase 3 (LH3, also known as PLOD3) into newly identified post-Golgi collagen IV carriers

  2. Proteomic analysis revealed that PLOD3, which is the gene encoding for collagen-modifying lysyl hydroxylase 3 (LH3), is regulated by miR-663a.

  3. The study shows that lysyl hydroxylase 3 localizes to epidermal basement membrane and is reduced in patients with recessive dystrophic epidermolysis bullosa.

  4. MMP-9 recruitment to the fibroblast cell surface by Lysyl Hydroxylase 3 (LH3) triggers TGF-beta activation and fibroblast differentiation

  5. LH3 molecules found in the cell medium are secreted through the Golgi complex, and the secretion is dependent on LH3 glycosyltransferase activity; LH3 found on the cell surface bypasses the Golgi complex

  6. Dimerization of human lysyl hydroxylase 3 is mediated by the amino acids 541-547

  7. Characterization of three fragments that constitute the monomers of the human lysyl hydroxylase isoenzymes 1-3. The 30-kDa N-terminal fragment is not required for lysyl hydroxylase activity

  8. Manipulation of the gene for LH3 can be used to selectively alter glycosylation and hydroxylation reactions, and provides new tool to clarify functions of unique hydroxylysine linked carbohydrates in collagens and other proteins.

  9. LH3 is present and active in the extracellular space

  10. The deficiency of LH3 glycosyltransferase activities, especially in the extracellular space, causes growth arrest.

  11. mutations of the lysyl hydroxylase 3 gene may cause a connective tissue disorder [case report]

PLOD3 profil antigène

Antigen Summary

The protein encoded by this gene is a membrane-bound homodimeric enzyme that is localized to the cisternae of the rough endoplasmic reticulum. The enzyme (cofactors iron and ascorbate) catalyzes the hydroxylation of lysyl residues in collagen-like peptides. The resultant hydroxylysyl groups are attachment sites for carbohydrates in collagen and thus are critical for the stability of intermolecular crosslinks. Some patients with Ehlers-Danlos syndrome type VIB have deficiencies in lysyl hydroxylase activity.

Gene names and symbols associated with PLOD3

  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 L homeolog (plod3.L) anticorps
  • procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 (PLOD3) anticorps
  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 (plod3) anticorps
  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 (PLOD3) anticorps
  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 (Plod3) anticorps
  • AI414586 anticorps
  • cb479 anticorps
  • cb816 anticorps
  • diwanka anticorps
  • DKFZp469I0226 anticorps
  • im:6912725 anticorps
  • LH3 anticorps
  • plod anticorps
  • PLOD3 anticorps
  • wu:fb72f10 anticorps

Protein level used designations for PLOD3

procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3 , procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 , diw , lh3 , procollagen-lysine,2-oxoglutarate 5-dioxygenase 3-like , lysyl hydroxylase 2 , lysyl hydroxylase 3 , LH3 , bone protein I (BP-I) , lysine hydroxylase 3 , lysyl hydroxlase 3

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514996 Bos taurus
556077 Danio rerio
734090 Xenopus (Silurana) tropicalis
100059479 Equus caballus
100173058 Pongo abelii
100390092 Callithrix jacchus
26433 Mus musculus
288583 Rattus norvegicus
8985 Homo sapiens
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