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MABE1103

Sigma-Aldrich

Anti-CST complex subunit CTC1 Antibody, clone C482

clone C482, from mouse

Synonim(y):

CST complex subunit CTC1, Conserved telomere maintenance component 1, HBV DNAPTP1-transactivated protein B

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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

C482, monoclonal

reaktywność gatunkowa

human

metody

western blot: suitable

izotyp

IgG2bκ

numer dostępu NCBI

numer dostępu UniProt

Warunki transportu

wet ice

docelowa modyfikacja potranslacyjna

unmodified

informacje o genach

human ... CTC1(80169)

Opis ogólny

CST complex subunit CTC1 (UniProt Q2NKJ3; also known as Conserved telomere maintenance component 1, HBV DNAPTP1-transactivated protein B) is encoded by the CTC1 (also known as C17orf68, CRMCC) gene (Gene ID 80169) in human. CTC1 is a subunit of the trimeric CST (CTC1, STN1, and TEN1) complex that binds ssDNA, promotes telomere DNA synthesis, and inhibits telomerase-mediated telomere elongation. CST directly interacts with and stimulates DNA polymerase -primase (pol -primase) activity. CST also associates with and sequesters telomeric 3′ overhangs after their elongation by telomerase, thereby limiting further telomere extension by telomerase. Knockdown of either STN1 or CCT1 in human cancer cells and in mouse fibroblasts results in substantially elongated telomeric G-ove+D13rhangs. Conditional deletion of CTC1 in mice leads to early entry into senescence and signs of telomeric replication defects, Human CTC1 gene mutations casue dyskeratosis congenita (DC) and related bone marrow failure syndromes, as well as the rare autosomal recessive neurological disorder Coats Plus, where patients develop cranial calcifications and cysts. Coats Plus and DC patients develop premature hair graying, anemia, and osteoporosis as a result of telomerase defects.

Specyficzność

Clone C482 targets an N-terminal region sequence present in both human CTC1 spliced isoforms reported by UniProt (Q2NKJ3).

Immunogen

Linear peptide corresponding to an N-terminal region sequence of human CTC1.

Zastosowanie

Anti-CST complex subunit CTC1, clone C482, Cat. No. MABE1103, is a highly specific mouse monoclonal antibody that targets CTC1 and has been tested in and Western Blotting.
Research Category
Epigenetics & Nuclear Function
Western Blotting Analysis: 0.75-1 µg/mL from a representative lot detected the exogenously overexpressed CTC1 in 100-150 ng of lysate from transfected HeLa cells, as well as downregulated CTC1 expression following conditional CTC1 gene knockout in 150 ng of lysate from a HCT116 cell line harboring floxed CTC1 alleles (Courtesy of Carolyn Price, Ph.D. and Xuyang Feng, Ph.D., University of Cincinnati College of Medicine, U.S.A.).

Jakość

Identity Confirmation by Isotyping Test.

Isotyping Analysis: The identity of this monoclonal antibody is confirmed by isotyping test to be IgG2b .

Opis wartości docelowych

~135 kDa observed. 134.61/114.1 kDa (isoform 1/2) calculated. Uncharacterized bands may be observed in some lysate(s).

Postać fizyczna

Format: Purified
Protein G purified.
Purified mouse IgG2b 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.
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Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 2


Certyfikaty analizy (CoA)

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Odwiedź Bibliotekę dokumentów

Xuyang Feng et al.
Nucleic acids research, 45(8), 4281-4293 (2017-03-24)
To prevent progressive telomere shortening as a result of conventional DNA replication, new telomeric DNA must be added onto the chromosome end. The de novo DNA synthesis involves elongation of the G-rich strand of the telomere by telomerase. In human

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