MSX1 monoclonal antibody (M11), clone 1E2

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Specification
Product Description
Mouse monoclonal antibody raised against a partial recombinant MSX1.
Immunogen
MSX1 (NP_002439, 216 a.a. ~ 297 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
Sequence
NRRAKAKRLQEAELEKLKMAAKPMLPPAAFGLSFPLGGPAAVAAAAGASLYGASGPFQRAALPVAPVGLYTAHVGYSMYHLT
Host
Mouse
Reactivity
Human, Mouse
Isotype
IgG2a Kappa
Quality Control Testing
Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (35.02 KDa) .
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 (Cell lysate)
MSX1 monoclonal antibody (M11), clone 1E2. Western Blot analysis of MSX1 expression in Raw 264.7.Western Blot (Cell lysate)
MSX1 monoclonal antibody (M11), clone 1E2. Western Blot analysis of MSX1 expression in U-2 OS.Western Blot (Recombinant protein)
Immunoprecipitation
Immunoprecipitation of MSX1 transfected lysate using anti-MSX1 monoclonal antibody and Protein A Magnetic Bead, and immunoblotted with MSX1 MaxPab rabbit polyclonal antibody.ELISA
Immunofluorescence
Immunofluorescence of monoclonal antibody to MSX1 on HeLa cell . [antibody concentration 10 ug/ml] -
Gene Info — MSX1
Entrez GeneID
4487GeneBank Accession#
NM_002448Protein Accession#
NP_002439Gene Name
MSX1
Gene Alias
HOX7, HYD1
Gene Description
msh homeobox 1
Gene Ontology
HyperlinkGene Summary
This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia. [provided by RefSeq
Other Designations
OTTHUMP00000115387|homeobox 7|msh homeo box 1|msh homeobox homolog 1
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Interactome
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Disease
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