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PLOD3 antibody (N-Term)
PLOD3
Reactivity: Human
WB, EIA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-PLOD3 Antibody
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Target
See all PLOD3 Antibodies
PLOD3
(Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase 3 (PLOD3))
Binding Specificity
All epitopes for PLOD3 antibodies
AA 85-113, N-Term
Reactivity
All reactivities for PLOD3 antibodies
Human
Host
All hosts for PLOD3 antibodies
Rabbit
Clonality
All clonalities for PLOD3 antibodies
Polyclonal
Conjugate
All conjugates for PLOD3 antibodies
This PLOD3 antibody is un-conjugated
Application
All applications for PLOD3 antibodies
Western Blotting (WB), Enzyme Immunoassay (EIA)
Specificity
This antibody recognizes Human PLOD3 (N-term).
Purification
Protein A column, followed by peptide affinity purification
Immunogen
KLH conjugated synthetic peptide between 85-113 amino acids from the N-terminal region of human PLOD3
Isotype
Ig Fraction
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Discover our top product PLOD3 Primary Antibody
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS containing 0.09 % (W/V) Sodium Azide as preservative
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Target Details for PLOD3
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Target
PLOD3
(Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase 3 (PLOD3))
Alternative Name
PLOD3 (PLOD3 Products )
Background
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.Synonyms: 2-oxoglutarate 5-dioxygenase 3, Lysyl hydroxylase 3, Procollagen-lysine
Molecular Weight
84785 Da
Gene ID
8985
NCBI Accession
NP_001075
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