ARFGAP3 Antibody Cat

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ARFGAP3 Antibody Cat. No.: 23-461 ARFGAP3 Antibody Immunohistochemistry of paraffin- embedded mouse stomach using Immunohistochemistry of paraffin-embedded human liver cancer using ARFGAP3 ARFGAP3 antibody (23-461) at antibody (23-461) at dilution of 1:100 (40x lens). dilution of 1:100 (40x lens). Immunohistochemistry of paraffin- embedded human esophagus using ARFGAP3 antibody (23-461) at dilution of 1:100 (40x lens). Specifications October 1, 2021 1 https://www.prosci-inc.com/arfgap3-antibody-23-461.html HOST SPECIES: Rabbit SPECIES REACTIVITY: Human, Mouse Recombinant fusion protein containing a sequence corresponding to amino acids 217-516 IMMUNOGEN: of human ARFGAP3 (NP_055385.3). TESTED APPLICATIONS: IHC, WB WB: ,1:500 - 1:2000 APPLICATIONS: IHC: ,1:50 - 1:100 POSITIVE CONTROL: 1) HepG2 2) Mouse pancreas PREDICTED MOLECULAR Observed: 57kDa WEIGHT: Properties PURIFICATION: Affinity purification CLONALITY: Polyclonal ISOTYPE: IgG CONJUGATE: Unconjugated PHYSICAL STATE: Liquid BUFFER: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. STORAGE CONDITIONS: Store at -20˚C. Avoid freeze / thaw cycles. Additional Info OFFICIAL SYMBOL: ARFGAP3 ARFGAP3, ADP-ribosylation factor GTPase activating protein 3, ARFGAP1, RP1-47A17.3, ALTERNATE NAMES: ADP-ribosylation factor GTPase activating protein 1, OTTHUMP00000028526 GENE ID: 26286 USER NOTE: Optimal dilutions for each application to be determined by the researcher. Background and References The protein encoded by this gene is a GTPase-activating protein (GAP) that associates with the Golgi apparatus and regulates the early secretory pathway of proteins. The encoded protein promotes hydrolysis of ADP-ribosylation factor 1 (ARF1)-bound GTP, which is required for the dissociation of coat proteins from Golgi-derived membranes and vesicles. BACKGROUND: Dissociation of the coat proteins is a prerequisite for the fusion of these vesicles with target compartments. The activity of this protein is sensitive to phospholipids. Multiple transcript variants encoding different isoforms have been found for this gene. This gene was originally known as ARFGAP1, but that is now the name of a related but different gene. October 1, 2021 2 https://www.prosci-inc.com/arfgap3-antibody-23-461.html ANTIBODIES FOR RESEARCH USE ONLY. For additional information, visit ProSci's Terms & Conditions Page. October 1, 2021 3 https://www.prosci-inc.com/arfgap3-antibody-23-461.html.

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Polyclonal Antibody to ARFGAP3 (C-Term) - Aff - Purified
OriGene Technologies, Inc. OriGene Technologies GmbH 9620 Medical Center Drive, Ste 200 Schillerstr. 5 Rockville, MD 20850 32052 Herford UNITED STATES GERMANY Phone: +1-888-267-4436 Phone: +49-5221-34606-0 Fax: +1-301-340-8606 Fax: +49-5221-34606-11 [email protected] [email protected] AP15932PU-N Polyclonal Antibody to ARFGAP3 (C-term) - Aff - Purified Alternate names: ADP-ribosylation factor GTPase-activating protein 3, ARF GAP 3, ARFGAP1 Quantity: 0.1 mg Concentration: 0.5 mg/ml Background: The protein encoded by this gene is a GTPase-activating protein (GAP) which associates with the Golgi apparatus and which is thought to interact with ADP- ribosylation factor 1 (ARF1). The encoded protein likely promotes hydrolysis of ARF1-bound GTP, which is required for the dissociation of coat proteins from Golgi- derived membranes and vesicles. Dissociation of the coat proteins is a prerequisite for the fusion of these vesicles with target compartments. The activity of this protein is sensitive to phospholipids. This gene was originally known as ARFGAP1, but that is now the name of a related but different gene. Uniprot ID: Q9NP61 NCBI: NP_055385.3 GeneID: 26286 Host: Goat Immunogen: Peptide from C Terminus of the protein sequence according to NP_055385.3; NP_001135765.1 Genename: ARFGAP3 AA Sequence: C-NGVVTSIQDRYGS Format: State: Liquid Ig fraction Purification: Ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide Buffer System: Tris saline, 0.02% sodium azide, pH7.3 with 0.5% bovine serum albumin Applications: Peptide ELISA: Limit dilution 1:8000. Western blot: 1-3 µg/ml.
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BMC Cell Biology Biomed Central
BMC Cell Biology BioMed Central Research article Open Access Mutational analysis of βCOP (Sec26p) identifies an appendage domain critical for function Carol J DeRegis1, Peter B Rahl2, Gregory R Hoffman3, Richard A Cerione4,5 and Ruth N Collins*4,6 Address: 1Graduate Program in Comparative Biomedical Sciences, Cornell University, Ithaca NY 14853, USA, 2Graduate Program in Pharmacology, Cornell University, Ithaca, NY 14853, USA, 3Graduate Program in Biophysics, Cornell University, Ithaca, NY 14853, USA, 4Department of Molecular Medicine, Cornell University, Ithaca, NY 14853, USA, 5Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853, USA and 6Department of Molecular Medicine, Cornell University, C4-109 Veterinary Medical Center, Ithaca, NY 14853, USA Email: Carol J DeRegis - [email protected]; Peter B Rahl - [email protected]; Gregory R Hoffman - [email protected]; Richard A Cerione - [email protected]; Ruth N Collins* - [email protected] * Corresponding author Published: 22 January 2008 Received: 2 June 2007 Accepted: 22 January 2008 BMC Cell Biology 2008, 9:3 doi:10.1186/1471-2121-9-3 This article is available from: http://www.biomedcentral.com/1471-2121/9/3 © 2008 De Regis et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: The appendage domain of the γCOP subunit of the COPI vesicle coat bears a striking structural resemblance to adaptin-family appendages despite limited primary sequence homology.
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Supplementary Materials
Supplementary materials Supplementary Table S1: MGNC compound library Ingredien Molecule Caco- Mol ID MW AlogP OB (%) BBB DL FASA- HL t Name Name 2 shengdi MOL012254 campesterol 400.8 7.63 37.58 1.34 0.98 0.7 0.21 20.2 shengdi MOL000519 coniferin 314.4 3.16 31.11 0.42 -0.2 0.3 0.27 74.6 beta- shengdi MOL000359 414.8 8.08 36.91 1.32 0.99 0.8 0.23 20.2 sitosterol pachymic shengdi MOL000289 528.9 6.54 33.63 0.1 -0.6 0.8 0 9.27 acid Poricoic acid shengdi MOL000291 484.7 5.64 30.52 -0.08 -0.9 0.8 0 8.67 B Chrysanthem shengdi MOL004492 585 8.24 38.72 0.51 -1 0.6 0.3 17.5 axanthin 20- shengdi MOL011455 Hexadecano 418.6 1.91 32.7 -0.24 -0.4 0.7 0.29 104 ylingenol huanglian MOL001454 berberine 336.4 3.45 36.86 1.24 0.57 0.8 0.19 6.57 huanglian MOL013352 Obacunone 454.6 2.68 43.29 0.01 -0.4 0.8 0.31 -13 huanglian MOL002894 berberrubine 322.4 3.2 35.74 1.07 0.17 0.7 0.24 6.46 huanglian MOL002897 epiberberine 336.4 3.45 43.09 1.17 0.4 0.8 0.19 6.1 huanglian MOL002903 (R)-Canadine 339.4 3.4 55.37 1.04 0.57 0.8 0.2 6.41 huanglian MOL002904 Berlambine 351.4 2.49 36.68 0.97 0.17 0.8 0.28 7.33 Corchorosid huanglian MOL002907 404.6 1.34 105 -0.91 -1.3 0.8 0.29 6.68 e A_qt Magnogrand huanglian MOL000622 266.4 1.18 63.71 0.02 -0.2 0.2 0.3 3.17 iolide huanglian MOL000762 Palmidin A 510.5 4.52 35.36 -0.38 -1.5 0.7 0.39 33.2 huanglian MOL000785 palmatine 352.4 3.65 64.6 1.33 0.37 0.7 0.13 2.25 huanglian MOL000098 quercetin 302.3 1.5 46.43 0.05 -0.8 0.3 0.38 14.4 huanglian MOL001458 coptisine 320.3 3.25 30.67 1.21 0.32 0.9 0.26 9.33 huanglian MOL002668 Worenine
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Gene Expression Profiling in Human Fetal Liver and Identification of Tissue
Downloaded from genome.cshlp.org on September 29, 2021 - Published by Cold Spring Harbor Laboratory Press Letter Gene Expression Profiling in Human Fetal Liver and Identification of Tissue- and Developmental-Stage-Specific Genes through Compiled Expression Profiles and Efficient Cloning of Full-Length cDNAs Yongtao Yu, Chenggang Zhang, Gangqiao Zhou, Songfeng Wu, Xianghu Qu, Handong Wei, Guichun Xing, Chunna Dong, Yun Zhai, Jinghong Wan, Shuguang Ouyang, Li Li, Shaowen Zhang, Kaixin Zhou, Yinan Zhang, Chutse Wu, and Fuchu He1 Department of Genomics and Proteomics, Beijing Institute of Radiation Medicine, Chinese National Human Genome Center at Beijing, Beijing 100850, China Fetal liver intriguingly consists of hepatic parenchymal cells and hematopoietic stem/progenitor cells. Human fetal liver aged 22 wk of gestation (HFL22w) corresponds to the turning point between immigration and emigration of the hematopoietic system. To gain further molecular insight into its developmental and functional characteristics, HFL22w was studied by generating expressed sequence tags (ESTs) and by analyzing the compiled expression profiles of liver at different developmental stages. A total of 13,077 ESTs were sequenced from a 3Ј-directed cDNA library of HFL22w, and classified as follows: 5819 (44.5%) matched to known genes; 5460 (41.8%) exhibited no significant homology to known genes; and the remaining 1798 (13.7%) were genomic sequences of unknown function, mitochondrial genomic sequences, or repetitive sequences. Integration of ESTs of known human genes generated a profile including 1660 genes that could be divided into 15 gene categories according to their functions. Genes related to general housekeeping, ESTs associated with hematopoiesis, and liver-specific genes were highly expressed.
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Datasheet: AHP697
Datasheet: AHP697 Description: GOAT ANTI HUMAN ARFGAP3 Specificity: ARFGAP3 Format: Purified Product Type: Polyclonal Antibody Isotype: Polyclonal IgG Quantity: 0.1 mg Product Details Applications This product has been reported to work in the following applications. This information is derived from testing within our laboratories, peer-reviewed publications or personal communications from the originators. Please refer to references indicated for further information. For general protocol recommendations, please visit www.bio-rad-antibodies.com/protocols. Yes No Not Determined Suggested Dilution Flow Cytometry Immunohistology - Frozen Immunohistology - Paraffin ELISA Immunoprecipitation Western Blotting 1ug/ml - 3ug/ml Where this antibody has not been tested for use in a particular technique this does not necessarily exclude its use in such procedures. Suggested working dilutions are given as a guide only. It is recommended that the user titrates the antibody for use in their own system using appropriate negative/positive controls. Target Species Human Species Cross Reacts with: Mouse Reactivity N.B. Antibody reactivity and working conditions may vary between species. Product Form Purified IgG - liquid Antiserum Preparation Antisera to ARFGAP3 were raised by repeated immunisations of goats with highly purified antigen. Purified IgG was prepared from whole serum by affinity chromatography. Buffer Solution TRIS buffered saline Preservative 0.02% Sodium Azide Stabilisers 0.5% Bovine Serum Albumin Approx. Protein IgG concentration 0.5 mg/ml Concentrations Immunogen Synthetic peptide NGVVTSIQDRYGS derived from C terminus of ARFGAP3 protein. Page 1 of 3 External Database Links UniProt: Q9NP61 Related reagents Entrez Gene: 26286 ARFGAP3 Related reagents Synonyms ARFGAP1 Specificity Goat anti ARFGAP3 recognises ARFGAP3 (ADP - ribosylation factor GTPase activating protein 3), originally described as ARFGAP1.
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The Arf1p Gtpase-Activating Protein Glo3p Executes Its Regulatory Function Through a Conserved Repeat Motif at Its C-Terminus
2604 Research Article The Arf1p GTPase-activating protein Glo3p executes its regulatory function through a conserved repeat motif at its C-terminus Natsuko Yahara1,*, Ken Sato1,2 and Akihiko Nakano1,3,‡ 1Molecular Membrane Biology Laboratory, RIKEN Discovery Research Institute and 2PRESTO, Japan Science and Technology Agency, Hirosawa, Wako, Saitama 351-0198, Japan 3Department of Biological Sciences, Graduate School of Science, University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan *Present address: Department of Biochemistry, University of Geneva, Sciences II, Geneva, Switzerland ‡Author for correspondence (e-mail: [email protected]) Accepted 21 March 2006 Journal of Cell Science 119, 2604-2612 Published by The Company of Biologists 2006 doi:10.1242/jcs.02997 Summary ADP-ribosylation factors (Arfs), key regulators of ArfGAP, Gcs1p, we have shown that the non-catalytic C- intracellular membrane traffic, are known to exert multiple terminal region of Glo3p is required for the suppression of roles in vesicular transport. We previously isolated eight the growth defect in the arf1 ts mutants. Interestingly, temperature-sensitive (ts) mutants of the yeast ARF1 gene, Glo3p and its homologues from other eukaryotes harbor a which showed allele-speciﬁc defects in protein transport, well-conserved repeated ISSxxxFG sequence near the C- and classiﬁed them into three groups of intragenic terminus, which is not found in Gcs1p and its homologues. complementation. In this study, we show that the We name this region the Glo3 motif and present evidence overexpression of Glo3p, one of the GTPase-activating that the motif is required for the function of Glo3p in vivo. proteins of Arf1p (ArfGAP), suppresses the ts growth of a particular group of the arf1 mutants (arf1-16 and arf1-17).
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Views See [6,25,26])
Wirthlin et al. BMC Genomics 2014, 15:1082 http://www.biomedcentral.com/1471-2164/15/1082 RESEARCH ARTICLE Open Access Comparative genomics reveals molecular features unique to the songbird lineage Morgan Wirthlin1, Peter V Lovell1, Erich D Jarvis2 and Claudio V Mello1* Abstract Background: Songbirds (oscine Passeriformes) are among the most diverse and successful vertebrate groups, comprising almost half of all known bird species. Identifying the genomic innovations that might be associated with this success, as well as with characteristic songbird traits such as vocal learning and the brain circuits that underlie this behavior, has proven difficult, in part due to the small number of avian genomes available until recently. Here we performed a comparative analysis of 48 avian genomes to identify genomic features that are unique to songbirds, as well as an initial assessment of function by investigating their tissue distribution and predicted protein domain structure. Results: Using BLAT alignments and gene synteny analysis, we curated a large set of Ensembl gene models that were annotated as novel or duplicated in the most commonly studied songbird, the Zebra finch (Taeniopygia guttata), and then extended this analysis to 47 additional avian and 4 non-avian genomes. We identified 10 novel genes uniquely present in songbird genomes. A refined map of chromosomal synteny disruptions in the Zebra finch genome revealed that the majority of these novel genes localized to regions of genomic instability associated with apparent chromosomal breakpoints. Analyses of in situ hybridization and RNA-seq data revealed that a subset of songbird-unique genes is expressed in the brain and/or other tissues, and that 2 of these (YTHDC2L1 and TMRA) are highly differentially expressed in vocal learning-associated nuclei relative to the rest of the brain.
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Figure S1. HAEC ROS Production and ML090 NOX5-Inhibition
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NRF1) Coordinates Changes in the Transcriptional and Chromatin Landscape Affecting Development and Progression of Invasive Breast Cancer
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Anti-Arfgap3 (RABBIT) Antibody - 100-401-H46
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University of Massachusetts Medical School eScholarship@UMMS Program in Molecular Medicine Publications and Presentations Program in Molecular Medicine 2019-05-15 ARF GTPases and their GEFs and GAPs: concepts and challenges Elizabeth Sztul University of Alabama, Birmingham Et al. Let us know how access to this document benefits ou.y Follow this and additional works at: https://escholarship.umassmed.edu/pmm_pp Part of the Amino Acids, Peptides, and Proteins Commons, Biochemistry Commons, Cell Biology Commons, Cells Commons, Enzymes and Coenzymes Commons, Molecular Biology Commons, and the Nucleic Acids, Nucleotides, and Nucleosides Commons Repository Citation Sztul E, Chen P, Casanova JE, Cherfils J, Dacks JB, Lambright DG, Lee FS, Randazzo PA, Santy LC, Schurmann A, Wilhelmi I, Yohe ME, Kahn RA. (2019). ARF GTPases and their GEFs and GAPs: concepts and challenges. Program in Molecular Medicine Publications and Presentations. https://doi.org/10.1091/ mbc.E18-12-0820. Retrieved from https://escholarship.umassmed.edu/pmm_pp/112 Creative Commons License This work is licensed under a Creative Commons Attribution-Noncommercial-Share Alike 3.0 License. This material is brought to you by eScholarship@UMMS. It has been accepted for inclusion in Program in Molecular Medicine Publications and Presentations by an authorized administrator of eScholarship@UMMS. For more information, please contact [email protected]. M BoC | PERSPECTIVE ARF GTPases and their GEFs and GAPs: concepts and challenges Elizabeth Sztula,†, Pei-Wen Chenb, James E. Casanovac, Jacqueline Cherfilsd, Joel B. Dackse, David G. Lambrightf, Fang-Jen S. Leeg, Paul A. Randazzoh, Lorraine C. Santyi, Annette Schürmannj, Ilka Wilhelmij, Marielle E. Yohek, and Richard A.
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