Anti-RBMS1 Monoclonal Antibody, Clone FQS0936(C) (DCABH-4025) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use

Anti-RBMS1 monoclonal antibody, clone FQS0936(C) (DCABH-4025) This product is for research use only and is not intended for diagnostic use. PRODUCT INFORMATION Product Overview Rabbit monoclonal to RBMS1 Antigen Description Single-stranded DNA binding protein that interacts with the region upstream of the MYC gene. Binds specifically to the DNA sequence motif 5-[AT]CT[AT][AT]T-3. Probably has a role in DNA replication. Immunogen Synthetic peptide (the amino acid sequence is considered to be commercially sensitive) (C terminal) Isotype IgG Source/Host Rabbit Species Reactivity Mouse, Rat, Human Clone FQS0936(C) Purity Tissue culture supernatant Conjugate Unconjugated Applications WB, IP Positive Control HeLa, HepG2, Jurkat, C6, Raw 264.7 and NIH3T3 cell lysates Format Liquid Size 100 μl Buffer Preservative: 0.01% Sodium azide; Constituents: 50% Glycerol, 0.05% BSA Preservative 0.01% Sodium Azide Storage Store at -20℃. Ship Shipped at 4°C. GENE INFORMATION 45-1 Ramsey Road, Shirley, NY 11967, USA Email: [email protected] Tel: 1-631-624-4882 Fax: 1-631-938-8221 1 © Creative Diagnostics All Rights Reserved Gene Name RBMS1 RNA binding motif, single stranded interacting protein 1 [ Homo sapiens ] Official Symbol RBMS1 Synonyms RBMS1; RNA binding motif, single stranded interacting protein 1; C2orf12, chromosome 2 open reading frame 12; RNA-binding motif, single-stranded-interacting protein 1; c myc gene single strand binding protein 2; DKFZp564H0764; HCC 4; MSSP 1; MSSP 2; MSSP Entrez Gene ID 5937 Protein Refseq NP_002888 UniProt ID P29558 Chromosome Location 2q24.2 Function DNA binding; RNA binding; double-stranded DNA binding; nucleotide binding; protein binding; single-stranded DNA binding; 45-1 Ramsey Road, Shirley, NY 11967, USA Email: [email protected] Tel: 1-631-624-4882 Fax: 1-631-938-8221 2 © Creative Diagnostics All Rights Reserved.

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New Approaches to Functional Process Discovery in HPV 16-Associated Cervical Cancer Cells by Gene Ontology
Cancer Research and Treatment 2003;35(4):304-313 New Approaches to Functional Process Discovery in HPV 16-Associated Cervical Cancer Cells by Gene Ontology Yong-Wan Kim, Ph.D.1, Min-Je Suh, M.S.1, Jin-Sik Bae, M.S.1, Su Mi Bae, M.S.1, Joo Hee Yoon, M.D.2, Soo Young Hur, M.D.2, Jae Hoon Kim, M.D.2, Duck Young Ro, M.D.2, Joon Mo Lee, M.D.2, Sung Eun Namkoong, M.D.2, Chong Kook Kim, Ph.D.3 and Woong Shick Ahn, M.D.2 1Catholic Research Institutes of Medical Science, 2Department of Obstetrics and Gynecology, College of Medicine, The Catholic University of Korea, Seoul; 3College of Pharmacy, Seoul National University, Seoul, Korea Purpose: This study utilized both mRNA differential significant genes of unknown function affected by the display and the Gene Ontology (GO) analysis to char- HPV-16-derived pathway. The GO analysis suggested that acterize the multiple interactions of a number of genes the cervical cancer cells underwent repression of the with gene expression profiles involved in the HPV-16- cancer-specific cell adhesive properties. Also, genes induced cervical carcinogenesis. belonging to DNA metabolism, such as DNA repair and Materials and Methods: mRNA differential displays, replication, were strongly down-regulated, whereas sig- with HPV-16 positive cervical cancer cell line (SiHa), and nificant increases were shown in the protein degradation normal human keratinocyte cell line (HaCaT) as a con- and synthesis. trol, were used. Each human gene has several biological Conclusion: The GO analysis can overcome the com- functions in the Gene Ontology; therefore, several func- plexity of the gene expression profile of the HPV-16- tions of each gene were chosen to establish a powerful associated pathway, identify several cancer-specific cel- cervical carcinogenesis pathway.
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