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PLOD1 antibody (C-Term)
This Rabbit Polyclonal antibody specifically detects PLOD1 in WB. It exhibits reactivity toward Human.
Quick Overview for PLOD1 antibody (C-Term) (ABIN5671398)
Target
See all PLOD1 Antibodies
PLOD1
(Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))
Reactivity
All reactivities for PLOD1 antibodies
Human
Host
All hosts for PLOD1 antibodies
Rabbit
Clonality
All clonalities for PLOD1 antibodies
Polyclonal
Conjugate
All conjugates for PLOD1 antibodies
This PLOD1 antibody is un-conjugated
Application
All applications for PLOD1 antibodies
Western Blotting (WB)
Product Details anti-PLOD1 Antibody
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Binding Specificity
All epitopes for PLOD1 antibodies
C-Term
Sequence
DLAFVVRYKP DEQPSLMPHH DASTFTINIA LNRVGVDYEG GGCRFLRYNC
Purification
Affinity purified
Immunogen
The immunogen is a synthetic peptide directed towards the C terminal region of human PLOD1
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
Buffer
Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
Target Details for PLOD1
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Target
PLOD1
(Procollagen-Lysine,2-Oxoglutarate 5-Dioxygenase 1 (PLOD1))
Alternative Name
PLOD1
Background
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. Two transcript variants encoding different isoforms have been found for this gene. Alias Symbols: LH, LH1, LLH, EDS6, PLOD Protein Size: 727
Gene ID
5351
NCBI Accession
NM_000302 , NP_000293
UniProt
Q02809
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