TDP1 Antikörper (AA 75-125)
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- Target Alle TDP1 Antikörper anzeigen
- TDP1 (Tyrosyl-DNA Phosphodiesterase 1 (TDP1))
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Bindungsspezifität
- AA 75-125
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser TDP1 Antikörper ist unkonjugiert
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Applikation
- Immunoprecipitation (IP)
- Verwendungszweck
- Rabbit anti-TDP1 Antibody, Affinity Purified
- Aufreinigung
- Affinity Purified
- Immunogen
- between AA 75 and 125
- Isotyp
- IgG
- Top Product
- Discover our top product TDP1 Primärantikörper
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- Applikationshinweise
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IP: 2 - 5 μg/mg lysate
WB: Not recommended. Use rabbit anti-TDP1 antibody ABIN7453800.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Konzentration
- 1000 μg/mL
- Buffer
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- 4 °C
- Haltbarkeit
- 12 months
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- Target
- TDP1 (Tyrosyl-DNA Phosphodiesterase 1 (TDP1))
- Andere Bezeichnung
- TDP1 (TDP1 Produkte)
- Hintergrund
- Background: Tyrosyl-DNA phosphodiesterase 1 (TDP1) is an enzyme that participates in the repair of DNA strand breaks associated with topoisomerase 1 (Top1) complexes. TDP1 catalyzes the removal of Top1 from DNA via the hydrolysis of the phosphodiester bond between the tyrosine residue of Top1 and the 3' phosphate of DNA. Removal of Top1 is then followed by DNA repair. TDP1 has been proposed to play more general roles in DNA damage repair independent of the Top1 complex. TDP1 has been shown to associate with DNA ligase IIIalpha, a component of the DNA single-stranded break repair (SSBR) machinery. It is also able to remove glycolate from 3'-phosphoglycolate termini of double-stranded breaks and a variety of other 3'- adducts. Defects in TDP1 are associated with spinocerebellar ataxia autosomal recessive with axonal neuropathy (SCAN1), a disease associated with peripheral axonal motor and sensory neuropathy and distal muscular atrophy.
- Gen-ID
- 55775
- NCBI Accession
- NP_001008744
- UniProt
- Q9NUW8
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