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Merck

T8573

Sigma-Aldrich

Monoclonal Anti-Topoisomerase I antibody produced in mouse

clone Mab1, purified immunoglobulin, buffered aqueous solution

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About This Item

MDL-Nummer:
UNSPSC-Code:
12352203
NACRES:
NA.41

Biologische Quelle

mouse

Konjugat

unconjugated

Antikörperform

purified immunoglobulin

Antikörper-Produkttyp

primary antibodies

Klon

Mab1, monoclonal

Form

buffered aqueous solution

Mol-Gew.

antigen ~100 kDa

Speziesreaktivität

human

Methode(n)

microarray: suitable
western blot: 1-2 μg/mL using A231 human kidney cells

Isotyp

IgG1

UniProt-Hinterlegungsnummer

Versandbedingung

dry ice

Lagertemp.

−20°C

Posttranslationale Modifikation Target

unmodified

Angaben zum Gen

human ... TOP1(7150)

Allgemeine Beschreibung

Monoclonal Anti-Topoisomerase I (mouse IgG1 isotype) is derived from the Mab1 hybridoma produced by the fusion of SP2/0 mouse myeloma cells and splenocytes from BALB/c mice immunized with human purified topoisomerase I. The protein family of DNA topoisomerases is divided into two types (type I and II). The type I enzymes include eukaryotic and bacterial topoisomerase I and III. Human DNA Topoisomerase I belong to the subtype IB enzymes. The protein has four distinct domains. There are four nuclear localization signals in the N-terminal domain. A linker domain of 77 amino acids follows the core domain. The fourth domain, which is 53 amino acids long, contains the active site Tyr723. Topoisomerase I (TOP1) gene is located on human chromosome 20q12.

Immunogen

purified human topoisomerase I

Anwendung

Monoclonal Anti-Topoisomerase I antibody produced in mouse has been used in western blot analysis.

Biochem./physiol. Wirkung

DNA topoisomerases are enzymes that control the amount of supercoiling in DNA. Without topoisomerases, DNA cannot replicate normally. Type I enzymes of DNA topoisomerases introduce transient single strand breaks in DNA. Recently it was reported that DNA topoisomerase I is involved in modulation of RNA and is present in retroviral particles, like human immunodeficiency virus (HIV1). Furthermore, the enzyme enhances HIV-1 cDNA production in reverse transcription assays in vitro. Topoisomerase I (TOP1) serves as swivel at the time of replication, transcription and recombination, which helps in releasing over winding of duplex DNA.

Physikalische Form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

Haftungsausschluss

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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Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

nwg

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Die Dokumentenbibliothek aufrufen

Mechanisms for defining supercoiling set point of DNA gyrase orthologs I. A nonconserved acidic C-terminal tail modulates Escherichia coli gyrase activity
Tretter EM and Berger JM
The Journal of Biological Chemistry, 287(22), 18636-18644 (2012)
Amygdalin inhibits genes related to cell cycle in SNU-C4 human colon cancer cells
Park HJ, et al.
World Journal of Gastroenterology, 11(33), 5156-5156 (2005)
DNA topoisomerase II and its growing repertoire of biological functions
Nitiss JL
Nature Reviews. Cancer, 9(5), 327-327 (2009)
Tanshinone IIA potentiates the efficacy of 5-FU in Colo205 colon cancer cells in vivo through downregulation of P-gp and LC3-II.
Su C C
Experimental and Therapeutic Medicine, 3(3), 555-559 (2012)
Chin-Cheng Su
Experimental and therapeutic medicine, 3(3), 555-559 (2012-09-13)
Traditional Chinese herbal medicines are widely accepted as an option for the treatment of colorectal cancers. Danshen (Salviae miltiorrhizae Radix) is widely prescribed in traditional Chinese medicine for cardiovascular diseases. Tanshinone IIA (Tan-IIA) is extracted from Danshen. Our previous studies

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