Leucine Proline-Enriched Proteoglycan (Leprecan) 1 (LEPRE1) ELISA Kits

LEPRE1 encodes an enzyme that is a member of the collagen prolyl hydroxylase family. Additionally we are shipping LEPRE1 Antibodies (48) and LEPRE1 Proteins (6) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
LEPRE1 64175 Q32P28
LEPRE1 114200 Q9R1J8
LEPRE1 56401 Q3V1T4
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Top LEPRE1 ELISA Kits at antibodies-online.com

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Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human
  96 Tests Log in to see 15 to 18 Days
$875.60
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Mouse
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$875.60
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Rat
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$875.60
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Chicken
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$1,095.60
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More ELISA Kits for LEPRE1 Interaction Partners

Human Leucine Proline-Enriched Proteoglycan (Leprecan) 1 (LEPRE1) interaction partners

  1. P3H1 mutation is associated with Non-Lethal Type VIII Osteogenesis Imperfecta (show COL1A2 ELISA Kits).

  2. This study enhances our knowledge about the mutational pattern of the LEPRE1, CRTAP (show CRTAP ELISA Kits), and PPIB (show PPIB ELISA Kits) genes. LEPRE1 should be the first gene analyzed in mutation detection studies in patients with recessive OI.

  3. An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.

  4. This is the first report of a mutation in LEPRE1 that eliminates only the KDEL ER-retrieval sequence, whereas other functional domains remain intact

  5. 0.4% of Mid-Atlantic African Americans and 1.48% West Africans carry mutation in LEPRE1 which causes lethal recessive osteogenesis imperfecta (show COL1A2 ELISA Kits).

  6. Mutation analyses were performed for COL1A1 (show COL1A1 ELISA Kits), COL1A2 (show COL1A2 ELISA Kits), CRTAP (show CRTAP ELISA Kits), and LEPRE1 in a cohort of 58 unrelated Chinese patients with osteogenesis imperfecta (show COL1A2 ELISA Kits).

  7. We report a large consanguineous Turkish family in which multiple individuals are affected with autosomal recessive lethal or severe osteogenesis imperfecta (show COL1A2 ELISA Kits) (OI) due to a novel homozygous LEPRE1 mutation

  8. Null mutations in LEPRE1 and CRTAP (show CRTAP ELISA Kits) cause severe recessive osteogenesis imperfecta (show COL1A2 ELISA Kits).

  9. CRTAP (show CRTAP ELISA Kits) and P3H1 are mutually stabilized in the collagen prolyl 3-hydroxylation complex in endoplasmic reticulum.

  10. Screening of 78 subjects diagnosed with osteogenesis imperfecta (show COL1A2 ELISA Kits) type II or III, identified three probands with mutations in CRTAP (show CRTAP ELISA Kits) and 16 with mutations in LEPRE1.

Mouse (Murine) Leucine Proline-Enriched Proteoglycan (Leprecan) 1 (LEPRE1) interaction partners

  1. P3H1 deficiency leads to decreased deposition of extracellular matrix by osteoblasts and increased incorporation of mineral into the matrix.

  2. we generated knock-in mice carrying a single amino acid substitution in the catalytic site of P3h1 (Lepre1(H662A) ). This substitution abolished P3h1 activity but retained ability to form a complex with Crtap (show CRTAP ELISA Kits) and thus the collagen chaperone

  3. An additional function of the rough endoplasmic reticulum protein complex prolyl 3-hydroxylase 1.cartilage-associated protein.cyclophilin B: the CXXXC motif reveals disulfide isomerase activity in vitro.

  4. The LEPRE1 knockout mouse is a valuable model system to investigate the mechanism of hearing loss in recessive osteogenesis imperfecta (show COL1A2 ELISA Kits).

  5. Prolyl 3-hydroxylase 1 null mice display abnormalities in fibrillar collagen-rich tissues such as tendons, skin, and bones

  6. Study found that all 3 mouse Leprecan genes Lepre1, leprel1 and leprel2 are expressed in the notochord; additionally, they are expressed in dorsal root ganglia, limb buds, branchial arches, and developing kidneys.

  7. This report characterizes expression of the P3H1, P3H2 and P3H3 genes in embryonic and adult mice.

LEPRE1 Antigen Profile

Antigen Summary

This gene encodes an enzyme that is a member of the collagen prolyl hydroxylase family. These enzymes are localized to the endoplasmic reticulum and their activity is required for proper collagen synthesis and assembly. Mutations in this gene are associated with osteogenesis imperfecta type VIII. Three alternatively spliced transcript variants encoding different isoforms have been described. Other variants may exist, but their biological validity has not been determined.

Gene names and symbols associated with LEPRE1

  • prolyl 3-hydroxylase 1 (P3H1) antibody
  • co-chaperonin GroES (groES) antibody
  • chaperonin GroS (groS1) antibody
  • 10 kDa chaperonin 1 (groS1) antibody
  • prolyl 3-hydroxylase 1 (P3h1) antibody
  • prolyl 3-hydroxylase 1 L homeolog (p3h1.L) antibody
  • prolyl 3-hydroxylase 1 (p3h1) antibody
  • 2410024C15Rik antibody
  • Gros1 antibody
  • LEPRE1 antibody
  • MGC84556 antibody
  • OI8 antibody
  • P3H1 antibody
  • sb:cb953 antibody

Protein level used designations for LEPRE1

growth suppressor 1 , leprecan , leucine- and proline-enriched proteoglycan 1 , prolyl 3-hydroxylase 1 , co-chaperonin GroES , chaperonin GroS , 10 kDa chaperonin 1 , growth supressor 1 , leprecan 1 , leprecan-1 , leprecan-1 homolog , leucine- and proline-enriched proteoglycan 1 homolog , leucine proline-enriched proteoglycan (leprecan) 1 , prolyl 3-hydroxylase 1-like

GENE ID SPECIES
64175 Homo sapiens
6933670 Burkholderia cenocepacia J2315
6941686 Thermodesulfovibrio yellowstonii DSM 11347
6988625 Aliivibrio salmonicida LFI1238
114200 Rattus norvegicus
414142 Gallus gallus
414447 Xenopus laevis
456811 Pan troglodytes
539976 Bos taurus
553321 Danio rerio
606980 Canis lupus familiaris
697917 Macaca mulatta
100036679 Xenopus (Silurana) tropicalis
100402370 Callithrix jacchus
100454619 Pongo abelii
100620503 Sus scrofa
56401 Mus musculus
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