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- Product number
- ABIN438414 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-rho GTPase Activating Protein 29 (ARHGAP29) (AA 1211-1261) antibody
- Antibody type
- Polyclonal
- Description
- Immunogen affinity purified
- Reactivity
- Human, Mouse
- Host
- Rabbit
- Epitope
- AA 1211-1261
- Vial size
- 100 μL
- Storage
- Store at 4°C. Do not freeze.
- Handling
- Do not freeze.
Submitted references ARHGAP29 Mutation Is Associated with Abnormal Oral Epithelial Adhesions.
MicroRNA-1291 promotes endometrial fibrosis by regulating the ArhGAP29-RhoA/ROCK1 signaling pathway in a murine model.
Rap1 Spatially Controls ArhGAP29 To Inhibit Rho Signaling during Endothelial Barrier Regulation.
Interferon regulatory factor 6 regulates keratinocyte migration.
Rasip1 mediates Rap1 regulation of Rho in endothelial barrier function through ArhGAP29.
Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
Paul BJ, Palmer K, Sharp JC, Pratt CH, Murray SA, Dunnwald M
Journal of dental research 2017 Oct;96(11):1298-1305
Journal of dental research 2017 Oct;96(11):1298-1305
MicroRNA-1291 promotes endometrial fibrosis by regulating the ArhGAP29-RhoA/ROCK1 signaling pathway in a murine model.
Xu Q, Duan H, Gan L, Liu X, Chen F, Shen X, Tang YQ, Wang S
Molecular medicine reports 2017 Oct;16(4):4501-4510
Molecular medicine reports 2017 Oct;16(4):4501-4510
Rap1 Spatially Controls ArhGAP29 To Inhibit Rho Signaling during Endothelial Barrier Regulation.
Post A, Pannekoek WJ, Ponsioen B, Vliem MJ, Bos JL
Molecular and cellular biology 2015 Jul;35(14):2495-502
Molecular and cellular biology 2015 Jul;35(14):2495-502
Interferon regulatory factor 6 regulates keratinocyte migration.
Biggs LC, Naridze RL, DeMali KA, Lusche DF, Kuhl S, Soll DR, Schutte BC, Dunnwald M
Journal of cell science 2014 Jul 1;127(Pt 13):2840-8
Journal of cell science 2014 Jul 1;127(Pt 13):2840-8
Rasip1 mediates Rap1 regulation of Rho in endothelial barrier function through ArhGAP29.
Post A, Pannekoek WJ, Ross SH, Verlaan I, Brouwer PM, Bos JL
Proceedings of the National Academy of Sciences of the United States of America 2013 Jul 9;110(28):11427-32
Proceedings of the National Academy of Sciences of the United States of America 2013 Jul 9;110(28):11427-32
Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
Leslie EJ, Mansilla MA, Biggs LC, Schuette K, Bullard S, Cooper M, Dunnwald M, Lidral AC, Marazita ML, Beaty TH, Murray JC
Birth defects research. Part A, Clinical and molecular teratology 2012 Nov;94(11):934-42
Birth defects research. Part A, Clinical and molecular teratology 2012 Nov;94(11):934-42
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