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AMMECR1 Antibody (C-term)

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
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  • WB - AMMECR1 Antibody (C-term) AW5605-U100
    All lanes : Anti-AMMECR1 Antibody (C-term) at 1:2000 dilution Lane 1: WiDr whole cell lysate Lane 2: A431 whole cell lysate Lane 3: MCF-7 whole cell lysate Lysates/proteins at 20 µg per lane. Secondary Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/10000 dilution. Predicted band size : 35 kDa Blocking/Dilution buffer: 5% NFDM/TBST.
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Product Information
Application
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
WB
Primary Accession Q9Y4X0
Other Accession Q9JHT5, Q5RAS7
Reactivity Human
Predicted Dog
Host Rabbit
Clonality Polyclonal
Calculated MW H=35,31,25;M=36 KDa
Isotype Rabbit IgG
Antigen Source HUMAN
Additional Information
Gene ID 9949
Antigen Region 271-298 aa
Other Names AMME syndrome candidate gene 1 protein, AMMECR1
Dilution WB~~1:2000
Target/Specificity This AMMECR1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 271-298 amino acids from the C-terminal region of human AMMECR1.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsAMMECR1 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name AMMECR1
Cellular Location Nucleus.
Research Areas
Citations (0)
citation

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Background

The exact function of this gene is not known, however, submicroscopic deletion of the X chromosome including this gene, COL4A5, and FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

References

Lamesch, P., et al. Genomics 89(3):307-315(2007)
Ross, M.T., et al. Nature 434(7031):325-337(2005)
Tajika, Y., et al. Proteins 58(2):501-503(2005)
Vitelli, F., et al. Genomics 55(3):335-340(1999)
Piccini, M., et al. Genomics 47(3):350-358(1998)

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$ 370.00
Cat# AW5605-U100
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