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Procollagen-lysine,2-oxoglutarate 5-dioxygenase

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Forms hydroxylysine residues in collagen type IV.

Below are the list of possible Procollagen-lysine,2-oxoglutarate 5-dioxygenase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Procollagen-lysine,2-oxoglutarate 5-dioxygenase

 Procollagen-lysine,2-oxoglutarate 5-dioxygenase ELISA Kit
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase Recombinant
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase Antibody
Also known as Procollagen-lysine,2-oxoglutarate 5-dioxygenase (Lethal protein 268) (Lysyl hydroxylase) (LH).
Forms hydroxylysine residues in collagen type IV.
 let-268 ELISA Kit
 let-268 Recombinant
 let-268 Antibody
 F52H3.1 ELISA Kit
 F52H3.1 Recombinant
 F52H3.1 Antibody
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Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1

 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 ELISA Kit
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 Recombinant
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 Antibody
Also known as Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 (Lysyl hydroxylase 1) (LH1).
Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens. These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links.
 PLOD1 ELISA Kit
 PLOD1 Recombinant
 PLOD1 Antibody
 PLOD ELISA Kit
 PLOD Recombinant
 PLOD Antibody
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Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2

 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 ELISA Kit
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 Recombinant
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 Antibody
Also known as Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 (Lysyl hydroxylase 2) (LH2).
PLOD2: Forms hydroxylysine residues in -Xaa-Lys-Gly- sequences in collagens. These hydroxylysines serve as sites of attachment for carbohydrate units and are essential for the stability of the intermolecular collagen cross-links. Defects in PLOD2 are the cause of Bruck syndrome type 2 (BRKS2). Bruck syn
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drome, also known as osteogenesis imperfecta with congenital joint contractures, is an autosomal recessive disease characterized by generalized osteopenia, joint contractures at birth, fragile bones and short stature. It can be distinguished from osteogenesis imperfecta by the absence of hearing loss and dentinogenesis imperfecta, and by the presence of clubfoot and congenital joint limitations. The molecular defect is an aberrant cross-linking of bone collagen, due to underhydroxylation of lysine residues within the telopeptides of type I collagen, whereas the lysine residues in the triple helix are normal. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Amino Acid Metabolism - lysine degradation; EC 1.14.11.4; Endoplasmic reticulum; Oxidoreductase

Chromosomal Location of Human Ortholog: 3q24

Cellular Component: endoplasmic reticulum; endoplasmic reticulum membrane

Molecular Function: procollagen-lysine 5-dioxygenase activity

Biological Process: protein modification process; response to hypoxia

Disease: Bruck Syndrome 2
 PLOD2 ELISA Kit
 PLOD2 Recombinant
 PLOD2 Antibody
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Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3

 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 ELISA Kit
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 Recombinant
 Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 Antibody
Also known as Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 (Lysyl hydroxylase 3) (LH3).
catalyzes hydroxylation of helical lysine residues and glycosylation of hydroxylysines in collagen; mediates collagen biosynthesis [RGD, Feb 2006]
 Plod3 ELISA Kit
 Plod3 Recombinant
 Plod3 Antibody
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