Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) ELISA Kits

Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the endoplasmic reticulum. Additionally we are shipping Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 Antibodies (36) and Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 Proteins (6) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
PLOD1 5351 Q02809
PLOD1 116552  
PLOD1 18822 Q9R0E2
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Top Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 ELISA Kits at antibodies-online.com

Showing 10 out of 16 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Delivery Price Details
Human 0.039 ng/mL 0.156-10 ng/mL Typical standard curve 96 Tests 15 to 18 Days
$910.56
Details
Rat 0.039 ng/mL 0.156-10 ng/mL Typical standard curve 96 Tests 15 to 18 Days
$910.56
Details
Monkey
  96 Tests 15 to 18 Days
$707.14
Details
Cow
  96 Tests 15 to 18 Days
$707.14
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Dog
  96 Tests 15 to 18 Days
$707.14
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Sheep
  96 Tests 15 to 18 Days
$707.14
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Pig
  96 Tests 15 to 18 Days
$707.14
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Chicken
  96 Tests 15 to 18 Days
$707.14
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Guinea Pig
  96 Tests 15 to 18 Days
$707.14
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Mouse
  96 Tests 15 to 18 Days
$707.14
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More ELISA Kits for Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 Interaction Partners

Human Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) interaction partners

  1. results indicated that PLOD1 is highly expressed in gastrointestinal carcinoma and is a potential prognostic marker and therapeutic target

  2. Ehlers Danlos syndrome in two children was confirmed by mutations in PLOD1 gene. Initially patients were thought to have either a diagnosis of classical EDS (cEDS) or a neuromuscular disorder due to absence of (congenital) scoliosis.

  3. Deficiency of the enzyme lysyl hydroxylase 1 (LH1) due to mutations in PLOD1 results in underhydroxylation of collagen lysyl residues and, hence, in the abnormal formation of collagen cross-links.

  4. Compared to slow progressing Alzheimer's disease, PLOD1 is upregulated in fast progressing Alzheimer's disease ;patients.

  5. Data show that homozygous and compound heterozygous changes found in PLOD1 and SLC2A10 may confer autosomal recessive effects, and three MYH11, ACTA2 and COL3A1 heterozygous variants were considered as putative pathogenic gene alterations.

  6. Common polymorphisms in four candidate genes (COL11A1, COL18A1, FBN1 and PLOD1) were unlikely to play important roles in the genetic susceptibility to high myopia.

  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. Results indicate that a C-terminal 40 amino acid segment of lysyl hydroxylase confers endoplasmic reticulum residency in a KDEL-receptor-independent manner.

  9. The results suggest that PLOD1 at 1p36, individually or in different combinations, contribute to osteoporosis susceptibility in Chinese.

Mouse (Murine) Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) interaction partners

  1. Plod1(-/-) mice offer an in vivo model for systematic analysis of the tissue-specific consequences of the lack of LH1 activity

Zebrafish Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) interaction partners

  1. Zebrafish lysyl hydroxylases 1 and 2 were cloned and their patterns of expression during the first two days of embryonic development examined.

Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1) Antigen Profile

Antigen Summary

Lysyl hydroxylase is a membrane-bound homodimeric protein localized to the cisternae of the 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 VI have deficiencies in lysyl hydroxylase activity.

Gene names and symbols associated with PLOD1

  • procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 (PLOD1) antibody
  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 (Plod1) antibody
  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 (PLOD1) antibody
  • procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 (Plod1) antibody
  • procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 (PLOD3) antibody
  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 L homeolog (plod1.L) antibody
  • procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1a (plod1a) antibody
  • 2410042F05Rik antibody
  • AI854890 antibody
  • AV007929 antibody
  • EDS6 antibody
  • ik:tdsubs_rzpd609-29b19 antibody
  • LH antibody
  • Lh1 antibody
  • LLH antibody
  • plod antibody
  • plod1 antibody
  • procollagen-lysine antibody
  • wu:fc29c10 antibody
  • wu:fc95g08 antibody
  • wu:fi18a05 antibody
  • zgc:152876 antibody

Protein level used designations for PLOD1

lysine hydroxylase , lysyl hydroxlase 1 , procollagen-lysine 1, 2-oxoglutarate 5-dioxygenase 1 , procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 , LH1 , lysyl hydroxylase 1 , procollagen-lysine 2-oxoglutarate 5-dioxygenase (lysine hydroxylase Ehlers-Danlos syndrome type VI) , procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase, Ehlers-Danlos syndrome type VI) , 2-oxoglutarate 5-dioxygenase 1 , procollagen-lysine 5-dioxygenase , procollagen-lysine 2-oxoglutarate 5-dioxygenase 1 , procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1 L homeolog , fc95g08 , fi18a05 , lh1 , procollagen lysine 2-oxoglutarate 5-dioxygenase 1 , procollagen-lysine 1, 2-oxoglutarate 5-dioxygenase 1a

GENE ID SPECIES
5351 Homo sapiens
116552 Rattus norvegicus
281409 Bos taurus
419485 Gallus gallus
18822 Mus musculus
100714306 Cavia porcellus
100861039 Capra hircus
100525583 Sus scrofa
101111306 Ovis aries
487440 Canis lupus familiaris
495112 Xenopus laevis
777635 Danio rerio
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