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>   home   >   Products   >   Primary Antibodies   >   Cell Biology   >   AMMECR1 Antibody (C-term)   

AMMECR1 Antibody (C-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

  • WB - AMMECR1 Antibody (C-term) AP19068b
    AMMECR1 Antibody (C-term) (Cat. #AP19068b) western blot analysis in WiDr cell line lysates (35ug/lane).This demonstrates the AMMECR1 antibody detected the AMMECR1 protein (arrow).
Product Information
  • 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
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q9Y4X0
Other Accession Q9JHT5, NP_001020751.1
Reactivity Human
Predicted Mouse
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 35463 Da
Antigen Region 271-298 aa
Additional Information
Gene ID 9949
Other Names AMME syndrome candidate gene 1 protein, AMMECR1
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.
Dilution WB~~1:1000
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
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
Research Areas
Citations (0)

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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.


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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$ 295.00
$ 99.00
Cat# AP19068b
(40 western blots)
Availability: In Stock
Bulk Size
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