JavaScript is disabled in your browser. Please enable JavaScript to view this website.
AB31751

Anti-PRMT5 抗体 - C-terminal

Anti-PRMT5 antibody - C-terminal

3

(4 Reviews)

|

(19 Publications)

Rabbit Polyclonal PRMT5 antibody. C-terminal. Suitable for WB and reacts with Human, Mouse samples. Cited in 19 publications.

別名を表示する

HRMT1L5, IBP72, JBP1, SKB1, PRMT5, Protein arginine N-methyltransferase 5, 72 kDa ICln-binding protein, Histone-arginine N-methyltransferase PRMT5, Jak-binding protein 1, Shk1 kinase-binding protein 1 homolog, SKB1 homolog, SKB1Hs

1 Images
Western blot - Anti-PRMT5 antibody - C-terminal (AB31751)
  • WB

Project

Western blot - Anti-PRMT5 antibody - C-terminal (AB31751)

All lanes:

Western blot - Anti-PRMT5 antibody - C-terminal (ab31751) at 1 µg/mL

Lane 1:

HL60 (Human promyelocytic leukemia cell line) whole cell lysate at 10 µg

Lane 2:

HEK-293 (Human embryonic kidney cell line) whole cell lysate at 10 µg

Lane 3:

Western blot - NIH/3T3 whole cell lysate (<a href='/products/cell-lysates/nih-3t3-whole-cell-lysate-ab7179'>ab7179</a>) at 10 µg

Secondary

All lanes:

Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution

Predicted band size: 73 kDa

Observed band size: 110 kDa,37 kDa,75 kDa

true

Exposure time: 6min

Key facts

宿主種

Rabbit

クローン性

Polyclonal

アイソタイプ

IgG

キャリアフリー

No

交差種

Mouse, Human

アプリケーション

WB

applications

免疫原

The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Human": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "1 µg/mL", "WB-species-notes": "<p>ab31751 shows weak staining in mouse samples.</p>" }, "Mouse": { "WB-species-checked": "guaranteed", "WB-species-dilution-info": "1 µg/mL", "WB-species-notes": "<p>ab31751 shows weak staining in mouse samples.</p>" }, "Xenopus laevis": { "WB-species-checked": "predicted", "WB-species-dilution-info": "", "WB-species-notes": "" }, "Zebrafish": { "WB-species-checked": "predicted", "WB-species-dilution-info": "", "WB-species-notes": "" } } }

出荷温度及び保存条件

製品の状態
Liquid
精製方法
Affinity purification Immunogen
バッファー組成
pH: 7.4 Preservative: 0.02% Sodium azide Constituents: PBS, 1% BSA
出荷温度
Blue Ice
短期保存期間
1-2 weeks
短期保存温度
+4°C
長期保存温度
-20°C
分注に関する情報
Upon delivery aliquot
保管に関する情報
Avoid freeze / thaw cycle

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

PRMT5 also known as Protein Arginine Methyltransferase 5 is an enzyme with molecular weight approximately 72 kDa. This protein catalyzes symmetric dimethylation of arginine residues on target proteins affecting gene expression and signal transduction. PRMT5 is expressed in various tissues with significant presence in the brain pancreas and lung. It enhances methyltransferase activity by interacting with other proteins and substrates.
Biological function summary

PRMT5 influences numerous cellular processes including RNA processing signal transduction and DNA repair. It functions as part of a protein complex often involving MEP50/WDR77 which modulates its methylating activity on histones and other proteins. This interaction dictates the cellular roles that are central to maintaining normal cellular function and regulation.

Pathways

PRMT5 operates within the Wnt/β-catenin signaling and mTOR pathways among others. As it modulates the methylation of transcription factors and regulators it contributes to transcriptional repression or activation which is important for cellular proliferation and differentiation. PRMT5 interacts with proteins such as Smad7 and cyclin D1 influencing these signaling pathways.

PRMT5 shows significant associations with cancer and neurological disorders. Elevated levels of PRMT5 correlate with the progression of various cancers including lung and breast cancers making it a potential target for therapeutic intervention. Additionally PRMT5's interaction with oncogenic proteins like MYC and MDM4 highlights its role in tumorigenesis. Furthermore PRMT5 dysregulation is linked to neurodegenerative diseases impacting the protein's target specificity and exacerbating disease symptoms.

製品プロトコール

For this product, it's our understanding that no specific protocols are required. You can visit:

ターゲットの情報

Arginine methyltransferase that can both catalyze the formation of omega-N monomethylarginine (MMA) and symmetrical dimethylarginine (sDMA), with a preference for the formation of MMA (PubMed : 10531356, PubMed : 11152681, PubMed : 11747828, PubMed : 12411503, PubMed : 15737618, PubMed : 17709427, PubMed : 20159986, PubMed : 20810653, PubMed : 21081503, PubMed : 21258366, PubMed : 21917714, PubMed : 22269951). Specifically mediates the symmetrical dimethylation of arginine residues in the small nuclear ribonucleoproteins Sm D1 (SNRPD1) and Sm D3 (SNRPD3); such methylation being required for the assembly and biogenesis of snRNP core particles (PubMed : 11747828, PubMed : 12411503, PubMed : 17709427). Methylates SUPT5H and may regulate its transcriptional elongation properties (PubMed : 12718890). May methylate the N-terminal region of MBD2 (PubMed : 16428440). Mono- and dimethylates arginine residues of myelin basic protein (MBP) in vitro. May play a role in cytokine-activated transduction pathways. Negatively regulates cyclin E1 promoter activity and cellular proliferation. Methylates histone H2A and H4 'Arg-3' during germ cell development (By similarity). Methylates histone H3 'Arg-8', which may repress transcription (By similarity). Methylates the Piwi proteins (PIWIL1, PIWIL2 and PIWIL4), methylation of Piwi proteins being required for the interaction with Tudor domain-containing proteins and subsequent localization to the meiotic nuage (By similarity). Methylates RPS10. Attenuates EGF signaling through the MAPK1/MAPK3 pathway acting at 2 levels. First, monomethylates EGFR; this enhances EGFR 'Tyr-1197' phosphorylation and PTPN6 recruitment, eventually leading to reduced SOS1 phosphorylation (PubMed : 21258366, PubMed : 21917714). Second, methylates RAF1 and probably BRAF, hence destabilizing these 2 signaling proteins and reducing their catalytic activity (PubMed : 21917714). Required for induction of E-selectin and VCAM-1, on the endothelial cells surface at sites of inflammation. Methylates HOXA9 (PubMed : 22269951). Methylates and regulates SRGAP2 which is involved in cell migration and differentiation (PubMed : 20810653). Acts as a transcriptional corepressor in CRY1-mediated repression of the core circadian component PER1 by regulating the H4R3 dimethylation at the PER1 promoter (By similarity). Methylates GM130/GOLGA2, regulating Golgi ribbon formation (PubMed : 20421892). Methylates H4R3 in genes involved in glioblastomagenesis in a CHTOP- and/or TET1-dependent manner (PubMed : 25284789). Symmetrically methylates POLR2A, a modification that allows the recruitment to POLR2A of proteins including SMN1/SMN2 and SETX. This is required for resolving RNA-DNA hybrids created by RNA polymerase II, that form R-loop in transcription terminal regions, an important step in proper transcription termination (PubMed : 26700805). Along with LYAR, binds the promoter of gamma-globin HBG1/HBG2 and represses its expression (PubMed : 25092918). Symmetrically methylates NCL (PubMed : 21081503). Methylates p53/TP53; methylation might possibly affect p53/TP53 target gene specificity (PubMed : 19011621). Involved in spliceosome maturation and mRNA splicing in prophase I spermatocytes through the catalysis of the symmetrical arginine dimethylation of SNRPB (small nuclear ribonucleoprotein-associated protein) and the interaction with tudor domain-containing protein TDRD6 (By similarity).
See full target information PRMT5

文献 (19)

Recent publications for all applications. Explore the full list and refine your search

Nature communications 13:5676 PubMed36167829

2022

TP53 mutations and RNA-binding protein MUSASHI-2 drive resistance to PRMT5-targeted therapy in B-cell lymphoma.

Applications

Unspecified application

Species

Unspecified reactive species

Tatiana Erazo,Chiara M Evans,Daniel Zakheim,Karen L Chu,Alice Yunsi Refermat,Zahra Asgari,Xuejing Yang,Mariana Da Silva Ferreira,Sanjoy Mehta,Marco Vincenzo Russo,Andrea Knezevic,Xi-Ping Zhang,Zhengming Chen,Myles Fennell,Ralph Garippa,Venkatraman Seshan,Elisa de Stanchina,Olena Barbash,Connie Lee Batlevi,Christina S Leslie,Ari M Melnick,Anas Younes,Michael G Kharas

Journal of immunology (Baltimore, Md. : 1950) 208:1525-1533 PubMed35288471

2022

PRMT5 in T Cells Drives Th17 Responses, Mixed Granulocytic Inflammation, and Severe Allergic Airway Inflammation.

Applications

Unspecified application

Species

Unspecified reactive species

Brandon W Lewis,Stephanie A Amici,Hye-Young Kim,Emily M Shalosky,Aiman Q Khan,Joshua Walum,Kymberly M Gowdy,Joshua A Englert,Ned A Porter,Mitchell H Grayson,Rodney D Britt,Mireia Guerau-de-Arellano

Molecular cell 81:3481-3495.e7 PubMed34358446

2021

Molecular basis for substrate recruitment to the PRMT5 methylosome.

Applications

Unspecified application

Species

Unspecified reactive species

Kathleen M Mulvaney,Christa Blomquist,Nischal Acharya,Ruitong Li,Matthew J Ranaghan,Meghan O'Keefe,Diego J Rodriguez,Michael J Young,Devishi Kesar,Debjani Pal,Matthew Stokes,Alissa J Nelson,Sidharth S Jain,Annan Yang,Zachary Mullin-Bernstein,Josie Columbus,Fazli K Bozal,Adam Skepner,Donald Raymond,Salvatore LaRussa,David C McKinney,Yelena Freyzon,Yossef Baidi,Dale Porter,Andrew J Aguirre,Alessandra Ianari,Brian McMillan,William R Sellers

Journal of medicinal chemistry 64:11148-11168 PubMed34342224

2021

Discovery of a First-in-Class Inhibitor of the PRMT5-Substrate Adaptor Interaction.

Applications

Unspecified application

Species

Unspecified reactive species

David C McKinney,Brian J McMillan,Matthew J Ranaghan,Jamie A Moroco,Merissa Brousseau,Zachary Mullin-Bernstein,Meghan O'Keefe,Patrick McCarren,Michael F Mesleh,Kathleen M Mulvaney,Foxy Robinson,Ritu Singh,Besnik Bajrami,Florence F Wagner,Robert Hilgraf,Martin J Drysdale,Arthur J Campbell,Adam Skepner,David E Timm,Dale Porter,Virendar K Kaushik,William R Sellers,Alessandra Ianari

Frontiers in immunology 12:695947 PubMed34168658

2021

PRMT5 Promotes Cyclin E1 and Cell Cycle Progression in CD4 Th1 Cells and Correlates With EAE Severity.

Applications

Unspecified application

Species

Unspecified reactive species

Stephanie A Amici,Wissam Osman,Mireia Guerau-de-Arellano

The Journal of clinical investigation 130:1683-1698 PubMed32091410

2020

Protein arginine methyltransferase 5 promotes cholesterol biosynthesis-mediated Th17 responses and autoimmunity.

Applications

Unspecified application

Species

Unspecified reactive species

Lindsay M Webb,Shouvonik Sengupta,Claudia Edell,Zayda L Piedra-Quintero,Stephanie A Amici,Janiret Narvaez Miranda,Makenzie Bevins,Austin Kennemer,Georgios Laliotis,Philip N Tsichlis,Mireia Guerau-de-Arellano

The Journal of endocrinology 244:41-52 PubMed31539871

2019

Islet-specific Prmt5 excision leads to reduced insulin expression and glucose intolerance in mice.

Applications

Unspecified application

Species

Unspecified reactive species

Jian Ma,Xin He,Yan Cao,Kienan O'Dwyer,Katherine M Szigety,Yuan Wu,Buddha Gurung,Zijie Feng,Bryson W Katona,Xianxin Hua

Frontiers in immunology 10:524 PubMed30941147

2019

NF-κB/mTOR/MYC Axis Drives PRMT5 Protein Induction After T Cell Activation via Transcriptional and Non-transcriptional Mechanisms.

Applications

Unspecified application

Species

Unspecified reactive species

Lindsay M Webb,Janiret Narvaez Miranda,Stephanie A Amici,Shouvonik Sengupta,Gregory Nagy,Mireia Guerau-de-Arellano

Oncotarget 9:33982-33994 PubMed30338040

2018

Sulforaphane inhibits growth and blocks Wnt/β-catenin signaling of colorectal cancer cells.

Applications

Unspecified application

Species

Unspecified reactive species

Dominic B Bernkopf,Gabriele Daum,Martina Brückner,Jürgen Behrens

Life science alliance 1:e201800070 PubMed30456350

2018

Proteomics and neuropathology identify ribosomes as poly-GR/PR interactors driving toxicity.

Applications

Unspecified application

Species

Unspecified reactive species

Hannelore Hartmann,Daniel Hornburg,Mareike Czuppa,Jakob Bader,Meike Michaelsen,Daniel Farny,Thomas Arzberger,Matthias Mann,Felix Meissner,Dieter Edbauer
View all publications

Abcam product promise

当社は、高品質な試薬を通じてお客様の研究を力強くサポートすることをお約束いたします。ご使用いただく各段階で、常にお客様をサポートできる体制を整えております。万が一、製品が期待通りに機能しない場合は、「Abcam Product Promise」による当社保証制度に基づき、安心してご利用いただけます。
保証に関する詳細については利用規約をご確認ください。

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

For licensing inquiries, please contact partnerships@abcam.com