MAOA MaxPab rabbit polyclonal antibody (D01)
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More Files
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human MAOA protein.
Immunogen
MAOA (NP_000231.1, 1 a.a. ~ 527 a.a) full-length human protein.
Sequence
MENQEKASIAGHMFDVVVIGGGISGLSAAKLLTEYGVSVLVLEARDRVGGRTYTIRNEHVDYVDVGGAYVGPTQNRILRLSKELGIETYKVNVSERLVQYVKGKTYPFRGAFPPVWNPIAYLDYNNLWRTIDNMGKEIPTDAPWEAQHADKWDKMTMKELIDKICWTKTARRFAYLFVNINVTSEPHEVSALWFLWYVKQCGGTTRIFSVTNGGQERKFVGGSGQVSERIMDLLGDQVKLNHPVTHVDQSSDNIIIETLNHEHYECKYVINAIPPTLTAKIHFRPELPAERNQLIQRLPMGAVIKCMMYYKEAFWKKKDYCGCMIIEDEDAPISITLDDTKPDGSLPAIMGFILARKADRLAKLHKEIRKKKICELYAKVLGSQEALHPVHYEEKNWCEEQYSGGCYTAYFPPGIMTQYGRVIRQPVGRIFFAGTETATKWSGYMEGAVEAGERAAREVLNGLGKVTEKDIWVQEPESKDVPAVEITHTFWERNLPSVSGLLKIIGFSTSVTALGFVLYKYKLLPRS
Host
Rabbit
Reactivity
Human
Interspecies Antigen Sequence
Mouse (88); Rat (88)
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
No additive
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Tissue lysate)
MAOA MaxPab rabbit polyclonal antibody. Western Blot analysis of MAOA expression in human placenta.Western Blot (Transfected lysate)
Western Blot analysis of MAOA expression in transfected 293T cell line (H00004128-T03) by MAOA MaxPab polyclonal antibody.
Lane 1: MAOA transfected lysate(59.70 KDa).
Lane 2: Non-transfected lysate.
Immunoprecipitation
Immunoprecipitation of MAOA transfected lysate using anti-MAOA MaxPab rabbit polyclonal antibody and Protein A Magnetic Bead, and immunoblotted with MAOA purified MaxPab mouse polyclonal antibody (B02P) (H00004128-B02P). -
Gene Info — MAOA
Entrez GeneID
4128GeneBank Accession#
NM_000240.2Protein Accession#
NP_000231.1Gene Name
MAOA
Gene Alias
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Gene Description
monoamine oxidase A
Omim ID
309850Gene Ontology
HyperlinkGene Summary
This gene encodes monoamine oxidase A, an enzyme that degrades amine neurotransmitters, such as dopamine, norepinephrine, and serotonin. The protein localizes to the mitochondrial outer membrane. The gene is adjacent to a related gene on the opposite strand of chromosome X. Mutation in this gene results in monoamine oxidase deficiency, or Brunner syndrome. [provided by RefSeq
Other Designations
OTTHUMP00000023165
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Interactome
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Pathway
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Disease
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