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PAX1 is a member of the paired box (PAX) family of transcription factors. Additionally we are shipping PAX1 Proteins (4) and many more products for this protein.
Showing 10 out of 88 products:
Human Polyclonal PAX1 Primary Antibody for EIA, FACS - ABIN954006
Huang, Lai, Liu, Lin, Wang, Ding, Chu: Quantitative analysis of methylation status of the PAX1 gene for detection of cervical cancer. in International journal of gynecological cancer : official journal of the International Gynecological Cancer Society 2010
Show all 5 references for ABIN954006
Human Polyclonal PAX1 Primary Antibody for EIA, WB - ABIN954007
Yerges, Klei, Cauley, Roeder, Kammerer, Moffett, Ensrud, Nestlerode, Marshall, Hoffman, Lewis, Lang, Barrett-Connor, Ferrell, Orwoll, Zmuda: High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009
Show all 5 references for ABIN954007
Human Polyclonal PAX1 Primary Antibody for WB - ABIN493215
Wallin, Wilting, Koseki, Fritsch, Christ, Balling: The role of Pax-1 in axial skeleton development. in Development (Cambridge, England) 1994
Show all 3 references for ABIN493215
Human Polyclonal PAX1 Primary Antibody for WB - ABIN655649
Richards, Yuan, Geller, Waterworth, Bataille, Glass, Song, Waeber, Vollenweider, Aben, Kiemeney, Walters, Soranzo, Thorsteinsdottir, Kong, Rafnar, Deloukas, Sulem, Stefansson, Stefansson, Spector, Mooser: Male-pattern baldness susceptibility locus at 20p11. in Nature genetics 2008
Human Polyclonal PAX1 Primary Antibody for WB - ABIN2778352
Vatanavicharn, Graham, Curry, Pepkowitz, Lachman, Rimoin, Wilcox: Diaphanospondylodysostosis: six new cases and exclusion of the candidate genes, PAX1 and MEOX1. in American journal of medical genetics. Part A 2007
Hypermethylation of PAX1 gene may be highly associated with the development of cervical cancer.
meta-analysis support the utility of PAX1 methylation as an auxiliary biomarker in cervical cancer screening
Testing PAX1 DNA methylation (show HELLS Antibodies) using oral swabs is a promising method for oral cancer detection. Combined assessments regarding betel nut consumption and DNA methylation (show HELLS Antibodies) can improve OSCC screening
PAX1 methylation hallmarks a potential diagnostic value for cervical cancer screening in Asians
analysis of a PAX1 enhancer locus that is associated with susceptibility to idiopathic scoliosis in females
PAX1 and SOX1 (show SOX1 Antibodies) DNA methylation (show HELLS Antibodies) correlate with a cervical intraepithelial neoplasia diagnosis.
PAX1 methylation is associated with cervical cancer.
PAX1 methylation is associated with high-grade squamous intraepithelial lesions.
Cervical adenocarcinoma cells carry aberrantly high methylation rates of PAX1, commonly methylated in squamous cell carcinomas.
We identified PAX1 as a novel disease-causing gene for otofaciocervical syndrome and show that the pooling of DNA from affected individuals can reduce the number of putative disease-causing homozygous variants in consanguineous families.
Cloning and examination through whole-mount in situ hybridization and reverse transcriptase-polymerase chain reaction of the expression patterns of pax1, pax9, and uncx transcription factors in the anuran Xenopus laevis.
Pax1 and Pax9 (show PAX9 Antibodies) can transactivate regulatory sequences in the Bapx1 (show NKX3-2 Antibodies) promoter to induce chondrogenic differentiation in the sclerotome.
Adult mice which carry a new allele of Pax1 have a lumbar scoliosis and kinky (show AXIN1 Antibodies) tails, a models for scoliosis
In addition to Hoxa3 (show HOXA3 Antibodies), this protein is required for both epithelial cell growth and differentiation throughout thymus and parathyroid organogenesis.
This gene is a member of the paired box (PAX) family of transcription factors. Members of the PAX family typically contain a paired box domain and a paired-type homeodomain. These genes play critical roles during fetal development. This gene plays a role in pattern formation during embryogenesis and may be essential for development of the vertebral column. This gene is silenced by methylation in ovarian and cervical cancers and may be a tumor suppressor gene. Mutations in this gene are also associated with vertebral malformations.
paired box 1
, paired box gene 1
, paired box protein Pax-1-like
, paired box protein Pax-1
, paired domain gene HuP48
, Paired box homeotic gene 1
, paired box protein 1
, paired box transcription factor
, wavy tail