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|Tested species reactivity||Mouse|
|Published species reactivity||Mouse|
|Host / Isotype||Mouse / IgG1, kappa|
|Immunogen||Synthetic peptide derived from the C-terminal region of the mouse Connexin 47 protein|
|Storage buffer||PBS, pH 7.4|
|Contains||0.1% sodium azide|
|Tested Applications||Dilution *|
|Immunofluorescence (IF)||Assay Dependent|
|Immunoprecipitation (IP)||Assay Dependent|
|Western Blot (WB)||Assay Dependent|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
This gene encodes a member of the gap junction protein family. The gap junction proteins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy. Alternatively spliced transcript variants encoding the same protein have been found for this gene.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
||Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans.||Tress O,Maglione M,Zlomuzica A,May D,Dicke N,Degen J,Dere E,Kettenmann H,Hartmann D,Willecke K||PLoS genetics (7:null)||2011|
|Mouse||Not Cited||Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans.||Tress O,Maglione M,Zlomuzica A,May D,Dicke N,Degen J,Dere E,Kettenmann H,Hartmann D,Willecke K||PLoS genetics (7:null)||2011|
|Mouse||2 µg/ml||Expression of zonula occludens-1 (ZO-1) and the transcription factor ZO-1-associated nucleic acid-binding protein (ZONAB)-MsY3 in glial cells and colocalization at oligodendrocyte and astrocyte gap junctions in mouse brain.||Penes MC,Li X,Nagy JI||The European journal of neuroscience (22:404)||2005|
|Mouse||Not Cited||Ablation of Cx47 in transgenic mice leads to the loss of MUPP1, ZONAB and multiple connexins at oligodendrocyte-astrocyte gap junctions.||Li X,Penes M,Odermatt B,Willecke K,Nagy JI||The European journal of neuroscience (28:1503)||2008|
connexin 47 type A; connexin 47 type C; connexin 47 type D; connexin-47; Cx46.6; Cx47; gap junction alpha-12 protein; gap junction gamma-2 protein; gap junction membrane channel protein alpha 12; gap junction protein, chi 2; GJA12; GJC2
B230382L12Rik; Cx47; Gja12; Gjc2