ACOX2 polyclonal antibody
* The price is valid only in USA. Please select country.
-
More Files
- More Functions
Western Blot (Tissue lysate)
ACOX2 polyclonal antibody (Cat # PAB7223) (0.1 ug/mL) staining of human liver lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
-
Specification
Product Description
Goat polyclonal antibody raised against synthetic peptide of ACOX2.
Immunogen
A synthetic peptide corresponding to human ACOX2.
Sequence
C-HQSRLRPSDPEAK
Host
Goat
Theoretical MW (kDa)
76.8
Reactivity
Human
Specificity
This antibody was designed using the mouse sequence, which differs by 1 amino acids (from the human sequence.
Form
Liquid
Purification
Antigen affinity purification
Concentration
0.5 mg/mL
Quality Control Testing
Antibody Reactive Against Synthetic Peptide.
Recommend Usage
ELISA (1:32000)
Western Blot (0.1-0.3 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
Storage Instruction
Store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Applications
Western Blot (Tissue lysate)
ACOX2 polyclonal antibody (Cat # PAB7223) (0.1 ug/mL) staining of human liver lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.Enzyme-linked Immunoabsorbent Assay
-
Gene Info — ACOX2
Entrez GeneID
8309Protein Accession#
NP_003491.1Gene Name
ACOX2
Gene Alias
BCOX, BRCACOX, BRCOX, THCCox
Gene Description
acyl-Coenzyme A oxidase 2, branched chain
Omim ID
601641Gene Ontology
HyperlinkGene Summary
The product of this gene belongs to the acyl-CoA oxidase family. It encodes the branched-chain acyl-CoA oxidase which is involved in the degradation of long branched fatty acids and bile acid intermediates in peroxisomes. Deficiency of this enzyme results in the accumulation of branched fatty acids and bile acid intermediates, and may lead to Zellweger syndrome, severe mental retardation, and death in children. [provided by RefSeq
Other Designations
Peroxisomal branched chain acyl-CoA oxidase|THCA-CoA oxidase|Trihydroxycoprostanoyl-CoA oxidase
-
Interactome
-
Pathway
-
Disease
-
Publication Reference
-
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome.
Baumgart E, Vanhooren JC, Fransen M, Marynen P, Puype M, Vandekerckhove J, Leunissen JA, Fahimi HD, Mannaerts GP, van Veldhoven PP.
PNAS 1996 Nov; 93(24):13748.
Application：WB-Re, Recombinant protein.
-
Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome.
- +1-909-264-1399
+1-909-992-0619
Toll Free : +1-877-853-6098 - +1-909-992-3401
- sales@abnova.com