CER1 Antibody (monoclonal) (M12)
Mouse monoclonal antibody raised against a full length recombinant CER1.
|Calculated MW||30084 Da|
|Other Names||Cerberus, Cerberus-related protein, DAN domain family member 4, CER1, DAND4|
|Target/Specificity||CER1 (NP_005445.1, 158 a.a. ~ 266 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.|
|Format||Clear, colorless solution in phosphate buffered saline, pH 7.2 .|
|Storage||Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.|
|Precautions||CER1 Antibody (monoclonal) (M12) is for research use only and not for use in diagnostic or therapeutic procedures.|
Thousands of laboratories across the world have published research that depended on the performance of antibodies from Abgent to advance their research. Check out links to articles that cite our products in major peer-reviewed journals, organized by research category.
email@example.com, and receive a free "I Love Antibodies" mug.
Provided below are standard protocols that you may find useful for product applications.
This gene encodes a cytokine member of the cysteine knot superfamily, characterized by nine conserved cysteines and a cysteine knot region. The cerberus-related cytokines, together with Dan and DRM/Gremlin, represent a group of bone morphogenetic protein (BMP) antagonists that can bind directly to BMPs and inhibit their activity.
A gene-based risk score for lung cancer susceptibility in smokers and ex-smokers. Young RP, et al. Postgrad Med J, 2009 Oct. PMID 19789190.High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. Yerges LM, et al. J Bone Miner Res, 2009 Dec. PMID 19453261.Lung cancer susceptibility model based on age, family history and genetic variants. Young RP, et al. PLoS One, 2009. PMID 19390575.Genome-wide haplotype association mapping in mice identifies a genetic variant in CER1 associated with BMD and fracture in southern Chinese women. Tang PL, et al. J Bone Miner Res, 2009 Jun. PMID 19113921.Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype. Swinkels ME, et al. Am J Med Genet A, 2008 Jun 1. PMID 18452192.
If you have used an Abgent product and would like to share how it has performed, please click on the "Submit Review" button and provide the requested information. Our staff will examine and post your review and contact you if needed.
If you have any additional inquiries please email technical services at firstname.lastname@example.org.