product summary
company name :
MilliporeSigma
other brands :
FLUKA, Sigma-Aldrich, Roche Applied Science
product type :
antibody
product name :
Monoclonal Anti-Polyglutamines antibody produced in mouse
catalog :
P1874
clonality :
monoclonal
host :
mouse
conjugate :
nonconjugated
clone name :
3B5H10
reactivity :
human, mouse
application :
western blot, immunoprecipitation
more info or order :
citations: 30
Published Application/Species/Sample/DilutionReference
  • western blot; mouse; 1:1000; loading ...; fig 7c
Juenemann K, Jansen A, van Riel L, Merkx R, Mulder M, An H, et al. Dynamic recruitment of ubiquitin to mutant huntingtin inclusion bodies. Sci Rep. 2018;8:1405 pubmed publisher
  • western blot; mouse; loading ...; fig 5c
Culver B, DeClercq J, Dolgalev I, Yu M, Ma B, Heguy A, et al. Huntington's Disease Protein Huntingtin Associates with its own mRNA. J Huntingtons Dis. 2016;5:39-51 pubmed publisher
  • western blot; mouse; 1:1000; fig 1
Yao Y, Cui X, Al Ramahi I, Sun X, Li B, Hou J, et al. A striatal-enriched intronic GPCR modulates huntingtin levels and toxicity. elife. 2015;4: pubmed publisher
  • immunoprecipitation; mouse
Sathasivam K, Neueder A, Gipson T, Landles C, Benjamin A, Bondulich M, et al. Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease. Proc Natl Acad Sci U S A. 2013;110:2366-70 pubmed publisher
Aviolat H, Pinto R, Godschall E, Murtha R, Richey H, Sapp E, et al. Assessing average somatic CAG repeat instability at the protein level. Sci Rep. 2019;9:19152 pubmed publisher
Li Z, Wang C, Wang Z, Zhu C, Li J, Sha T, et al. Allele-selective lowering of mutant HTT protein by HTT-LC3 linker compounds. Nature. 2019;: pubmed publisher
Kourkouta E, Weij R, González Barriga A, Mulder M, Verheul R, Bosgra S, et al. Suppression of Mutant Protein Expression in SCA3 and SCA1 Mice Using a CAG Repeat-Targeting Antisense Oligonucleotide. Mol Ther Nucleic Acids. 2019;17:601-614 pubmed publisher
Imanikia S, Sheng M, Castro C, Griffin J, Taylor R. XBP-1 Remodels Lipid Metabolism to Extend Longevity. Cell Rep. 2019;28:581-589.e4 pubmed publisher
Imanikia S, Özbey N, Krueger C, Casanueva M, Taylor R. Neuronal XBP-1 Activates Intestinal Lysosomes to Improve Proteostasis in C. elegans. Curr Biol. 2019;29:2322-2338.e7 pubmed publisher
Franich N, Hickey M, Zhu C, Osborne G, Ali N, Chu T, et al. Phenotype onset in Huntington's disease knock-in mice is correlated with the incomplete splicing of the mutant huntingtin gene. J Neurosci Res. 2019;97:1590-1605 pubmed publisher
Tousley A, Iuliano M, Weisman E, Sapp E, Zhang N, Vodicka P, et al. Rac1 Activity Is Modulated by Huntingtin and Dysregulated in Models of Huntington's Disease. J Huntingtons Dis. 2019;8:53-69 pubmed publisher
Baldo B, Sajjad M, Cheong R, Bigarreau J, Vijayvargia R, McLean C, et al. Quantification of Total and Mutant Huntingtin Protein Levels in Biospecimens Using a Novel alphaLISA Assay. Eneuro. 2018;5: pubmed publisher
Neueder A, Dumas A, Benjamin A, Bates G. Regulatory mechanisms of incomplete huntingtin mRNA splicing. Nat Commun. 2018;9:3955 pubmed publisher
Mani R, Gupta M, Malik A, Tandon R, Prasad R, Bhatnagar R, et al. Adjuvant Potential of Poly-α-l-Glutamine from the Cell Wall of Mycobacterium tuberculosis. Infect Immun. 2018;86: pubmed publisher
Ghosh D, Roy A, Ranjan A. The ATPase VCP/p97 functions as a disaggregase against toxic Huntingtin-exon1 aggregates. FEBS Lett. 2018;592:2680-2692 pubmed publisher
Vidinska D, Vochozková P, Šmatlíková P, Ardan T, Klima J, Juhás S, et al. Gradual Phenotype Development in Huntington Disease Transgenic Minipig Model at 24 Months of Age. Neurodegener Dis. 2018;18:107-119 pubmed publisher
Clift D, McEwan W, Labzin L, Konieczny V, Mogessie B, James L, et al. A Method for the Acute and Rapid Degradation of Endogenous Proteins. Cell. 2017;171:1692-1706.e18 pubmed publisher
Yu M, Fu Y, Liang Y, Song H, Yao Y, Wu P, et al. Suppression of MAPK11 or HIPK3 reduces mutant Huntingtin levels in Huntington's disease models. Cell Res. 2017;27:1441-1465 pubmed publisher
Rindt H, Tom C, Lorson C, Mattis V. Optimization of trans-Splicing for Huntington's Disease RNA Therapy. Front Neurosci. 2017;11:544 pubmed publisher
Lee A, Ung H, Sands L, Kikis E. A new Caenorhabditis elegans model of human huntingtin 513 aggregation and toxicity in body wall muscles. PLoS ONE. 2017;12:e0173644 pubmed publisher
Pavel M, Imarisio S, Menzies F, Jimenez Sanchez M, Siddiqi F, Wu X, et al. CCT complex restricts neuropathogenic protein aggregation via autophagy. Nat Commun. 2016;7:13821 pubmed publisher
Zhang X, Abels E, Redzic J, Margulis J, Finkbeiner S, Breakefield X. Potential Transfer of Polyglutamine and CAG-Repeat RNA in Extracellular Vesicles in Huntington's Disease: Background and Evaluation in Cell Culture. Cell Mol Neurobiol. 2016;36:459-70 pubmed publisher
Stroedicke M, Bounab Y, Strempel N, Klockmeier K, Yigit S, Friedrich R, et al. Systematic interaction network filtering identifies CRMP1 as a novel suppressor of huntingtin misfolding and neurotoxicity. Genome Res. 2015;25:701-13 pubmed publisher
Fodale V, Kegulian N, Verani M, Cariulo C, Azzollini L, Petricca L, et al. Polyglutamine- and temperature-dependent conformational rigidity in mutant huntingtin revealed by immunoassays and circular dichroism spectroscopy. PLoS ONE. 2014;9:e112262 pubmed publisher
Landles C, Weiss A, Franklin S, Howland D, Bates G. Caspase-6 does not contribute to the proteolysis of mutant huntingtin in the HdhQ150 knock-in mouse model of Huntington's disease. PLoS Curr. 2012;4:e4fd085bfc9973 pubmed publisher
Vidal R, Figueroa A, Court F, Thielen P, Molina C, Wirth C, et al. Targeting the UPR transcription factor XBP1 protects against Huntington's disease through the regulation of FoxO1 and autophagy. Hum Mol Genet. 2012;21:2245-62 pubmed publisher
Prahlad V, Morimoto R. Neuronal circuitry regulates the response of Caenorhabditis elegans to misfolded proteins. Proc Natl Acad Sci U S A. 2011;108:14204-9 pubmed publisher
Thompson L, Aiken C, Kaltenbach L, Agrawal N, Illes K, Khoshnan A, et al. IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome. J Cell Biol. 2009;187:1083-99 pubmed publisher
Wacker J, Zareie M, Fong H, Sarikaya M, Muchowski P. Hsp70 and Hsp40 attenuate formation of spherical and annular polyglutamine oligomers by partitioning monomer. Nat Struct Mol Biol. 2004;11:1215-22 pubmed
Brooks E, Arrasate M, Cheung K, Finkbeiner S. Using antibodies to analyze polyglutamine stretches. Methods Mol Biol. 2004;277:103-28 pubmed
product information
Product No. :
P1874
Product Name :
Monoclonal Anti-Polyglutamines antibody produced in mouse
Host :
mouse
Conjugate :
unconjugated
Antibody Type :
monoclonal
Clone Number (if monoclonal) :
3B5H10
Applications/Description :
Suitable for immunocytochemistry; western blot: 1-2 μg/mL using extract of HEK-293T cells transfected with an N-terminal 171 amino acid fragment of human Huntingtin with a 68 glutamine stretch; immunoprecipitation (IP)
Species Reactivity :
human
Isotype :
IgG1
Concentration :
~2 mg/mL
Storage :
Store at -20°C
more info or order :
company information
MilliporeSigma
PO Box 14508
St. Louis, MO 63178
https://www.sigmaaldrich.com
1-800-325-3010
headquarters: USA