CERU rabbit pAb
The protein encoded by this gene is a metalloprotein that binds most of the copper in plasma and is involved in the peroxidation of Fe (II)transferrin to Fe (III) transferrin. Mutations in this gene cause aceruloplasminemia, which results in iron accumulation and tissue damage, and is associated with diabetes and neurologic abnormalities. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Feb 2012],
Product Specifications
Background
UniProt
P00450
Swiss Prot
P00450
Reactivity
Human; Rat; Mouse
Immunogen
Synthesized peptide derived from part region of human protein
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Molecular Weight
117kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
117kD
Fragment
IgG
Subcellular Location
Secreted. Colocalizes with GCP1 in secretory intracellular compartments. .
Gene ID (Human)
1356
Available Sizes
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