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ANTXR2 / CMG2 Antibody (internal regoin)

Peptide-affinity purified goat antibody

  • WB - ANTXR2 / CMG2 Antibody (internal regoin) AF3179a
    AF3179a (0.3 µg/ml) staining of Mouse Kidney lysate (35 µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
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 P58335
Other Accession NP_477520.2, NP_001139266.1, 118429
Reactivity Human, Mouse, Rat
Predicted Dog, Cow
Host Goat
Clonality Polyclonal
Concentration 0.5 mg/ml
Isotype IgG
Calculated MW 53666 Da
Additional Information
Gene ID 118429
Other Names Anthrax toxin receptor 2, Capillary morphogenesis gene 2 protein, CMG-2, ANTXR2, CMG2
Format 0.5 mg/ml in Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsANTXR2 / CMG2 Antibody (internal regoin) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Synonyms CMG2
Function Necessary for cellular interactions with laminin and the extracellular matrix.
Cellular Location Isoform 1: Cell membrane; Single-pass type I membrane protein. Note=Expressed at the cell surface Isoform 3: Secreted.
Tissue Location Expressed in prostate, thymus, ovary, testis, pancreas, colon, heart, kidney, lung, liver, peripheral blood leukocytes, placenta, skeletal muscle, small intestine and spleen
Research Areas
Citations (0)

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This antibody is expected to recognize both reported isoforms (NP_477520.2; NP_001139266.1).


Systemic hyalinosis mutations in the CMG2 ectodomain leading to loss of function through retention in the endoplasmic reticulum. Deuquet J, Abrami L, Difeo A, Ramirez MC, Martignetti JA, van der Goot FG, Human mutation 2009 Apr 30 (4): 583-9. PMID: 19191226

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$ 325.00
Cat# AF3179a
(40 western blots)
Availability: 7-10 days
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