Lysine Hydroxylase 2/PLOD2 Antibody (C1) - BSA Free

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Western Blot: Lysine Hydroxylase 2/PLOD2 Antibody (C1) [NBP3-41656] - Sample: Human Serum Primary Ab: 2ug/ml NBP3-41656; Second Ab: 0.2ug/mL HRP-Linked Caprine Anti-Mouse IgG Polyclonal Antibody

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB
Clone
C1
Clonality
Monoclonal
Host
Mouse
Conjugate
Unconjugated
Format
BSA Free
Concentration
1 mg/ml

Order Details

Lysine Hydroxylase 2/PLOD2 Antibody (C1) - BSA Free Summary

Description
Novus Biologicals Mouse Lysine Hydroxylase 2/PLOD2 Antibody (C1) - BSA Free (NBP3-41656) is a monoclonal antibody validated for use in WB. All Novus Biologicals antibodies are covered by our 100% guarantee.
Immunogen
Immunized with recombinant Human Lysine Hydroxylase 2/PLOD2 (Uniprot#: O00469; Lys644-Pro737 (Uniprot#: O00469)
Isotype
IgG1 Kappa
Clonality
Monoclonal
Host
Mouse
Gene
PLOD2
Purity
Protein A or G purified
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • Western Blot 0.5-2ug/mL

Packaging, Storage & Formulations

Storage
Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
Buffer
0.01M PBS, pH7.4, 50% glycerol
Preservative
0.05% Proclin 300
Concentration
1 mg/ml
Purity
Protein A or G purified

Alternate Names for Lysine Hydroxylase 2/PLOD2 Antibody (C1) - BSA Free

  • 2-oxoglutarate 5-dioxygenase (lysine hydroxylase) 2
  • 2-oxoglutarate 5-dioxygenase 2
  • LH2
  • Lysine Hydroxylase 2
  • PLOD2
  • procollagen-lysine
  • telopeptide lysyl hydroxylase
  • TLH

Background

PLOD2 is 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. Mutations in the coding region of this gene are associated with Bruck syndrome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Bioinformatics

Gene Symbol PLOD2