MABE1031
Anti-poly-ADP-ribose binding reagent
Anti-poly-ADP-ribose binding reagent is a reagent that selectively binds to ADP ribose for use in Western Blotting, Immunocytochemistry and Dot Blot.
Sinônimo(s):
poly-ADP-ribose binding reagent
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About This Item
Código UNSPSC:
12352203
eCl@ss:
32160405
NACRES:
NA.41
Produtos recomendados
fonte biológica
Escherichia coli
Nível de qualidade
forma do anticorpo
purified antibody
tipo de produto de anticorpo
primary antibodies
reatividade de espécies
human, mouse
reatividade da espécie (prevista por homologia)
all
técnica(s)
dot blot: suitable
immunocytochemistry: suitable
western blot: suitable
Condições de expedição
dry ice
modificação pós-traducional do alvo
unmodified
Descrição geral
Cat. No. MABE1031, Anti-poly-ADP-ribose binding reagent, is a His-tagged recombinant protein fused to rabbit Fc tag, expressed in and purified from Rosetta(DE3)pLysS strain of E. coli (Cat. No. 70956). Anti-poly-ADP-ribose binding reagent is useful for the affinity detection of oligo- and poly-ADP-ribosylated (PARylated) proteins on membranes or on fixed cells in a manner similar to antibody-based Western blot, dot blot, and immunocytochemistry applications. The rabbit Fc tag allows visualization of the binding/labeling with conjugated anti-rabbit secondary antibodies. The Fc tag also allows Anti-poly-ADP-ribose binding reagent to be captured on Protein A resins for affinity pull-down applications.
Especificidade
Two or more units of ADP-ribose
Aplicação
Anti-poly-ADP-ribose binding reagent is a reagent that selectively binds to ADP ribose for use in Western Blotting, Immunocytochemistry and Dot Blot.
Dot Blot Specificity Analysis: This reagent detected oligo(ADPR) and poly(ADPR) on ADP-ribosylated PARP1 recombinant protein (Lee Kraus, University of Texas Southwestern Medical Center).
Immunocytochemistry Analysis: A representative lot detected oligo(ADPR) and poly(ADPR)/PAR in 3T3-L1 cells (Lee Kraus, University of Texas Southwestern Medical Center).
Immunocytochemistry Analysis: A representative lot detected oligo(ADPR) and poly(ADPR)/PAR in 3T3-L1 cells (Lee Kraus, University of Texas Southwestern Medical Center).
Research Category
Epigenetics & Nuclear Function
Epigenetics & Nuclear Function
Research Sub Category
General Post-translation Modification
General Post-translation Modification
Qualidade
Evaluated by Western Blotting on ADP-ribosylated PARP1 and PARP3 recombinant proteins.
Western Blotting Analysis: This reagent detected oligo(ADPR) and poly(ADPR) on ADP-ribosylated PARP1 recombinant protein (Lee Kraus, University of Texas Southwestern Medical Center).
Western Blotting Analysis: This reagent detected oligo(ADPR) and poly(ADPR) on ADP-ribosylated PARP1 recombinant protein (Lee Kraus, University of Texas Southwestern Medical Center).
Descrição-alvo
Variable depending on the target proteins and the extend of ADP-ribosylation
forma física
Format: Purified
Ni-NTA agarose
Purified from E. coli by Ni-NTA agarose. Supplied in buffer containing 10 mM Tris pH 7.5, 0.2 M NaCl, 10% Glycerol, 10 mM Imidazole, 1 mM PMSF, 1 mM β-Mercaptoethanol, 10% glycerol without preservatives.
Armazenamento e estabilidade
Stable for 1 year at -80°C from date of receipt.
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 -80°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
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 -80°C. Avoid repeated freeze/thaw cycles, which may damage IgG and affect product performance.
Outras notas
Concentration: Please refer to lot specific datasheet.
Exoneração de responsabilidade
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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Código de classe de armazenamento
12 - Non Combustible Liquids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Certificados de análise (COA)
Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.
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Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
George E Ronson et al.
Nature communications, 9(1), 746-746 (2018-02-23)
PARP1 regulates the repair of DNA single-strand breaks generated directly, or during base excision repair (BER). However, the role of PARP2 in these and other repair mechanisms is unknown. Here, we report a requirement for PARP2 in stabilising replication forks
Tom P Aird et al.
American journal of physiology. Endocrinology and metabolism, 321(6), E802-E820 (2021-11-09)
Sprint interval training (SIT) is a time-efficient alternative to endurance exercise, conferring beneficial skeletal muscle metabolic adaptations. Current literature has investigated the nutritional regulation of acute and chronic exercise-induced metabolic adaptations in muscle following endurance exercise, principally comparing the impact
Dragomir B Krastev et al.
Nature communications, 9(1), 2016-2016 (2018-05-24)
Poly (ADP-ribose)ylation is a dynamic protein modification that regulates multiple cellular processes. Here, we describe a system for identifying and characterizing PARylation events that exploits the ability of a PBZ (PAR-binding zinc finger) protein domain to bind PAR with high-affinity.
Xin Luo et al.
Molecular cell, 65(2), 260-271 (2017-01-21)
Poly(ADP-ribosyl)ation (PARylation) is a post-translational modification of proteins mediated by PARP family members, such as PARP-1. Although PARylation has been studied extensively, few examples of definitive biological roles for site-specific PARylation have been reported. Here we show that C/EBPβ, a key
Xiao-Nan Zhang et al.
Nature communications, 10(1), 4196-4196 (2019-09-15)
Nicotinamide adenine dinucleotide (NAD+)-dependent ADP-ribosylation plays important roles in physiology and pathophysiology. It has been challenging to study this key type of enzymatic post-translational modification in particular for protein poly-ADP-ribosylation (PARylation). Here we explore chemical and chemoenzymatic synthesis of NAD+
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