AMBN purified MaxPab mouse polyclonal antibody (B01P)
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More Files
- More Functions
Western Blot (Transfected lysate)
Western Blot analysis of AMBN expression in transfected 293T cell line by AMBN MaxPab polyclonal antibody.
Lane 1: AMBN transfected lysate(49.17 KDa).
Lane 2: Non-transfected lysate.
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Specification
Product Description
Mouse polyclonal antibody raised against a full-length human AMBN protein.
Immunogen
AMBN (NP_057603.1, 1 a.a. ~ 447 a.a) full-length human protein.
Sequence
MSASKIPLFKMKDLILILCLLEMSFAVPFFPQQSGTPGMASLSLETMRQLGSLQRLNTLSQYSRYGFGKSFNSLWMHGLLPPHSSLPWMRPREHETQQYEYSLPVHPPPLPSQPSLKPQQPGLKPFLQSAAATTNQATALKEALQPPIHLGHLPLQEGELPLVQQQVAPSDKPPKPELPGVDFADPQGPSLPGMDFPDPQGPSLPGLDFADPQGSTIFQIARLISHGPMPQNKQSPLYPGMLYVPFGANQLNAPARLGIMSSEEVAGGREDPMAYGAMFPGFGGMRPGFEGMPHNPAMGGDFTLEFDSPVAATKGPENEEGGAQGSPMPEANPDNLENPAFLTELEPAPHAGLLALPKDDIPGLPRSPSGKMKGLPSVTPAAADPLMTPELADVYRTYDADMTTSVDFQEEATMDTTMAPNSLQTSMPGNKAQEPEMMHDAWHFQEP
Host
Mouse
Reactivity
Human
Interspecies Antigen Sequence
Mouse (58); Rat (61)
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of AMBN expression in transfected 293T cell line by AMBN MaxPab polyclonal antibody.
Lane 1: AMBN transfected lysate(49.17 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — AMBN
Entrez GeneID
258GeneBank Accession#
NM_016519Protein Accession#
NP_057603.1Gene Name
AMBN
Gene Alias
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Gene Description
ameloblastin (enamel matrix protein)
Omim ID
601259Gene Ontology
HyperlinkGene Summary
Ameloblastin is thought to represent an unique ameloblast-specific gene product that may be important in enamel matrix formation and mineralization. The gene is located on chromosome 4 near other genes associated with mineralized tissues: osteopontin, bone sialoprotein, and bone morphogenetic protein 3. Based on its cytogenetic location, this gene is a candidate gene for one form of the disorder, dentinogenesis imperfecta, and/or the disorder, autosomal dominant amylogenesis imperfecta. [provided by RefSeq
Other Designations
ameloblastin
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Interactome
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Disease
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