Przejdź do zawartości
Merck
Wszystkie zdjęcia(5)

Kluczowe dokumenty

MABE1112

Sigma-Aldrich

Anti-PRMT9 Antibody, clone 128-29-1

clone 128-29-1, from mouse

Synonim(y):

Putative protein arginine N-methyltransferase 9, Putative protein arginine N-methyltransferase 10

Zaloguj sięWyświetlanie cen organizacyjnych i kontraktowych


About This Item

Kod UNSPSC:
12352203
eCl@ss:
32160702
NACRES:
NA.41

pochodzenie biologiczne

mouse

Poziom jakości

forma przeciwciała

purified immunoglobulin

rodzaj przeciwciała

primary antibodies

klon

128-29-1, monoclonal

reaktywność gatunkowa

human

spodziewany brak reakcji z

mouse

metody

immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

izotyp

IgG1κ

numer dostępu NCBI

numer dostępu UniProt

docelowa modyfikacja potranslacyjna

unmodified

informacje o genach

human ... PRMT9(90826)

Opis ogólny

Putative protein arginine N-methyltransferase 9 (UniProt Q6P2P2; also known as Putative protein arginine N-methyltransferase 10) is encoded by the PRMT9 (also known as PRMT10) gene (Gene ID 90826) in human. Mammalian protein arginine methyltransferases (PRMTs) catalyze the methylation of arginine residues on histone and non-histone proteins. PRMTs are divided into three types based on their mode of activity. Type I PRMTs (PRMT1–4, PRMT6, and PRMT8) transfer up to two methyl groups on the same terminal guanidino nitrogen of arginine to form ω-NG-monomethylarginine (MMA) and ω-NG,NG-asymmetric dimethylarginine (ADMA) residues. Type II PRMTs (PRMT5 and PRMT9) transfer methyl groups on different terminal guanidino nitrogens to form ΜΜΑ and ω-NG,N′G-symmetric dimethylarginine (SDMA) residues, while type III PRMT7 transfers only one single methyl group to form MMA residues. PRMT9 is involved in alternative splicing regulation by modulating spliceosomal small nuclear ribonucleoprotein (snRNP) maturation in the cytoplasm. PRMT9 complexes with the splicing factors SF3B2 (SAP145) and SF3B4 (SAP49) and mediates SF3B2 Arg508 modification via MMA and SDMA. Similar to PRMT7, but unlike other PRMTs, PRMT9 contains a duplicated methyltransferase domain (a.a. 137-446 and 530-845), with the N-terminal MTase acting as a funtional AdoMet-binding domain and the C-terminal MTase domain serving a pseudodimer function, mimicking the homodimer formation of other PRMTs needed for subtrate processing. In addition, PRMT9 contains three tetratricopeptide repeats (TPR1-3; a.a. 25-58, 67-100, 101-134) known to mediate protein-protein interactions.

Specyficzność

Clone detected GST fusion containing recombinant human PRMT9 fragment a.a. 401-550, as well as endogenous human, but not mouse, PRMT9 in cell lysates (Yang, Y., et al. (2015). Nat. Commun. 6:6428). Epitope region is present in both spliced isoforms of human PRMT9 reported by UniProt (Q6P2P2).

Immunogen

Epitope: First MTase domain.
GST-tagged recombinant protein corresponding to the N-terminal half of human PRMT9.

Zastosowanie

Anti-PRMT9 Antibody, clone 128-29-1 is an antibody against PRMT9 for use in Western Blotting, Immunohistochemistry, Immunoprecipitation, Immunocytochemistry.
Research Category
Epigenetics & Nuclear Function
Research Sub Category
General Post-translation Modification
Western Blotting Analysis: 2.0 µg/mL from a representative lot detected PRMT9 in 20 µg of HeLa cell lysate.
Immunohistochemistry Analysis: A 1:50 dilution from a representative lot detected PRMT9 in human kidney, testis, and cerebellum tissue sections.
Immunocytochemistry Analysis: A representative lot detected a predominant cyotoplasmic PRMT9 localization by fluorescent immunocytochemistry staining of 4% paraformaldehyde-fixed HeLa cells (Yang, Y., et al. (2015). Nat. Commun. 6:6428).
Immunoprecipitation Analysis: A representative lot immunoprecipitated PRMT9 from HeLa cell lysates (Yang, Y., et al. (2015). Nat. Commun. 6:6428).
Western Blotting Analysis: A representative lot detected GST fusion protein containing human PRMT9 a.a. 401-550 recombinant fragment, but not PRMT9 a.a. 1-199, 200-400, or 551-895 GST fusion (Yang, Y., et al. (2015). Nat. Commun. 6:6428).
Western Blotting Analysis: A representative lot detected human, but not mouse, PRMT9 using lysates from various human and mouse cell lines (Yang, Y., et al. (2015). Nat. Commun. 6:6428).

Jakość

Evaluated by Western Blotting in A431 cell lysate.

Western Blotting Analysis: 2.0 µg/mL of this antibody detected PRMT9 in 20 µg of A431 cell lysate.

Opis wartości docelowych

~94 kDa observed. 94.50 kDa (isoform 1) and 81.86 kDa (isoform 2) calculated. Uncharacterized band(s) may appear in some lysates.

Postać fizyczna

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Przechowywanie i stabilność

Stable for 1 year at 2-8°C from date of receipt.

Inne uwagi

Concentration: Please refer to lot specific datasheet.

Oświadczenie o zrzeczeniu się odpowiedzialności

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Ta strona może zawierać tekst przetłumaczony maszynowo.

Nie możesz znaleźć właściwego produktu?  

Wypróbuj nasz Narzędzie selektora produktów.

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 1

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Ishita Rehman et al.
Nucleic acids research, 46(11), 5601-5617 (2018-05-03)
Human tyrosyl-DNA phosphodiesterases (TDP) hydrolyze the phosphodiester bond between DNA and the catalytic tyrosine of Top1 to excise topoisomerase I cleavage complexes (Top1cc) that are trapped by camptothecin (CPT) and by genotoxic DNA alterations. Here we show that the protein

Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.

Skontaktuj się z zespołem ds. pomocy technicznej