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MAB1286-I

Sigma-Aldrich

Anti-Nuclear Spliceosomes Antibody, clone 780-3

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About This Item

Kod UNSPSC:
12352203
NACRES:
NA.41
białko sprzężone:
unconjugated
application:
EM
FACS
IF
WB
klon:
780-3, monoclonal
reaktywność gatunkowa:
human
citations:
metody:
electron microscopy: suitable
flow cytometry: suitable
immunofluorescence: suitable
western blot: suitable

pochodzenie biologiczne

mouse

Poziom jakości

białko sprzężone

unconjugated

forma przeciwciała

purified antibody

rodzaj przeciwciała

primary antibodies

klon

780-3, monoclonal

reaktywność gatunkowa

human

opakowanie

antibody small pack of 100 μg

metody

electron microscopy: suitable
flow cytometry: suitable
immunofluorescence: suitable
western blot: suitable

izotyp

IgMκ

sekwencja epitopowa

Unknown

numer dostępu Protein ID

Unknown

Warunki transportu

dry ice

docelowa modyfikacja potranslacyjna

unmodified

Opis ogólny

Most eukaryotic genes are expressed as pre-mRNAs that are converted to mRNA by splicing. In this process noncoding sequences (introns) are removed, and coding sequences (exons) are ligated together. Some exons are known to be constitutively spliced and are present in every mRNA produced from a given pre-mRNA. However, many are alternatively spliced to generate variable forms of mRNA from a single pre-mRNA species. Nuclear pre-mRNA splicing is catalyzed by the spliceosome that is a multi-megadalton ribonucleoprotein (RNP) complex. It removes introns from nuclear pre-mRNA. The conformation and composition of spliceosome is shown to be dynamic, which is critical for its high degree of accuracy and flexibility. In most eukaryotes two unique spliceosomes have been described: the U2 -dependent spliceosome that catalyzes the removal of U2-type of introns and the U12-dependent spliceosome that is present only in a subset of eukaryotes and splices U12-type of intron. Introns are removed by two consecutive transesterification reactions. In the first reaction the 2 OH group of the branch adenosine of the intron carries out a nucleophilic attack on the 5 ss, which results in cleavage at this site and ligation of the 5 end of the intron to the branch adenosine, forming a lariat structure. In the second reaction, the 3 ss is attacked by the 3 OH group of the 5 exon, which leads to the ligation of the 5 and 3 exons forming the mRNA, and release of the intron. (Ref.: Matera, AG., and Wang, Z. (2014). Nat. Rev. Mol. Cell Biol. 15(2); 108-121; Will, CL., and Luhrmann, R. (2011). Cold Spring Harb. Perspect. Biol. 3(7); a003707; Patel, AA., and Steitz, JA. (2003). Nat. Rev. Mol. Cell Biol. 4(12); 960-970).

Specyficzność

Clone 780-3 is a mouse monoclonal antibody that detects human Nuclear spliceosomes.

Immunogen

Nuclear preparation from U266 human myeloma cells.

Zastosowanie

Quality Control Testing

Evaluated by Flow Cytometry in permeabilized HeLa cells.

Flow Cytometry Analysis: 2 μg of this antibody detected Nuclear Spliceosomes in one million permeabilized HeLa cells.

Tested Applications

Flow Cytometry Analysis: A representative lot detected Nuclear Spliceosomes in Flow Cytometry applications (Clevenger, C.V., et al. (1985). Cytometry. 6(3): 208-14; Bauer, K.D., et al. (1986). Cancer Res. 46(5): 2428-34; Clevenger, C.V., et al. (1987). Cytometry. 8(3): 280-6).

Immunofluorescence Analysis: A representative lot detected Nuclear Spliceosomes in Immunofluorescence applications (Clevenger, C.V., et al. (1984). J Histochem Cytochem. 32(7): 757-65; Clevenger, C.V., et al. (1985). Cytometry. 6(3): 208-14; Bauer, K.D., et al. (1986). Cancer Res. 46(5): 2428-34; Clevenger, C.V., et al. (1987). Cytometry. 8(3):280-6; Clevenger, C.V., et al. (1987). Cytometry. 8(3): 280-6).

Western Blotting Analysis: A representative lot detected Nuclear Spliceosomes in Western Blotting applications (Clevenger, C.V., et al. (1987). Cytometry. 8(3): 280-6; Kumar, P., et al. (2012). PLoS One. 7(8): e42712).

Electron Microscopy: A representative lot detected Nuclear Spliceosomes in Electron Microscopy applications (Clevenger, C.V., et al. (1984). J Histochem Cytochem. 32(7): 757-65; Bauer, K.D., et al. (1986). Cancer Res. 46(5): 2428-34; Clevenger, C.V., et al. (1987). Cytometry. 8(3): 280-6).

Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Anti-Nuclear Spliceosomes, clone 780-3, Cat. No. MAB1286-I, is a mouse monoclonal antibody that detects Nuclear spliceosomes and is tested for use in Electron Microscopy, Flow Cytometry, Immunofluorescence, and Western Blotting.

Postać fizyczna

Purified mouse monoclonal antibody IgM in PBS without preservatives.

Przechowywanie i stabilność

Store at -10°C to -25°C. Handling Recommendations: Upon receipt and prior to removing the cap, centrifuge the vial and gently mix the solution. Aliquot into microcentrifuge tubes and store at -20°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.

Inne uwagi

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

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.
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Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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