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AB221820

NMNAT1 Activity Assay Kit (Colorimetric)

NMNAT1 Activity Assay Kit (Colorimetric)

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(1 Publication)

NMNAT1 Activity Assay Kit (Colorimetric) (ab221820) provides a sensitive and robust method to evaluate activators and inhibitors of nicotinamide mononucleotide adenylyltransferase (NMNAT) activity using recombinant NMNAT protein or purified NMNAT protein.

別名を表示する

NMNAT, NMNAT1, Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1, NMN/NaMN adenylyltransferase 1, Nicotinamide-nucleotide adenylyltransferase 1, Nicotinate-nucleotide adenylyltransferase 1, NMN adenylyltransferase 1, NaMN adenylyltransferase 1

3 Images
Functional Studies - NMNAT1 Activity Assay Kit (Colorimetric) (AB221820)
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Supplier Data

Functional Studies - NMNAT1 Activity Assay Kit (Colorimetric) (AB221820)

NMNAT1 Activity Assay Kit (Colorimetric) (ab221820) Time course kinetic curve of recombinant NMNAT activity using One-Step Assay Method

Functional Studies - NMNAT1 Activity Assay Kit (Colorimetric) (AB221820)
  • FuncS

Supplier Data

Functional Studies - NMNAT1 Activity Assay Kit (Colorimetric) (AB221820)

NMNAT1 Activity Assay Kit (Colorimetric) (ab221820). Inhibitory effect of Gallotannin on recombinant NMNAT activity using One-Step Assay Method

Functional Studies - NMNAT1 Activity Assay Kit (Colorimetric) (AB221820)
  • FuncS

Supplier Data

Functional Studies - NMNAT1 Activity Assay Kit (Colorimetric) (AB221820)

NMNAT1 Activity Assay Kit (Colorimetric) (ab221820) Measurement of NMNAT activity on immunoprecipitated cell lysates from Raji cell extracts. Normal rabbit IgG control shows background activity compard to anti-NMNAT1 immunoprecipitate.

Key facts

検出方法

Colorimetric

サンプルタイプ

Purified protein, Recombinant Protein

Semi-Quantitative
アッセイプラットフォーム

Microplate reader

Reactivity data

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製品の詳細

NMNAT1 Activity Assay Kit (Colorimetric) (ab221820) provides a sensitive and robust method to evaluate activators and inhibitors of nicotinamide mononucleotide adenylyltransferase (NMNAT) activity using recombinant NMNAT protein. The assay can also be used to measure activity from endogenous NMNAT immunoprecipitated from cell extracts. The assay is based on a multi-step reaction that converts WST-1 to WST-1 formazan, which can be easily detected at OD 450 nm. As the reaction is not stopped, it is necessary to monitor the absorbance increase of WST-1 formazan at OD450 nm at regular intervals after the reaction is initiated to determine velocity of reaction.

Detection of NMNAT activity can be measured with a One-Step or a Two-Step method. For the One-Step method, the four enzymes involved in the reaction are mixed together. The detection sensitivity of this method is lower than that of the Two-Step method since three coupled reactions occur simultaneously. We recommend performing the One-step assay only when using purified protein. The Two-Step method is performed by adding the first two enzymes to produce NAD+, followed by the addition of the rest of the components to form WST-1 formazan by NAD/NADH enzyme cycling reaction. We recommend performing the Two-Step assay if using immunoprecipitated cell lysates, as the assay procedure allows to check for contamination and interference for NAD+ present in the sample. Since the assay is based on a NAD+ detection system, it is not possible to directly detect NMNAT activity in crude cell extracts, which contain relatively high NAD+.

For the One-Step method, we describe a procedure to test NMNAT activity using purified enzyme and a separate procedure for screening NAMPT activity inhibitors. For the Two-Step Method, we describe two different procedures to test NMNAT activity using purified enzyme or to test immunoprecipitated cell lysates. There is also a separate procedure for screening NMNAT activity inhibitors.

Nicotinamide mononucleotide adenylyltransferase 1 (NMNAT1, EC 2.7.7.1) is a central enzyme in NAD+ biosynthesis, transferring the adenylyl moiety of ATP to β-Nicotinamide mononucleotide (NMN) or nicotinic acid mononucleotide (NaMN), resulting in the formation of NAD+ or NaAD and the release of pyrophosphate. This enzyme could be a potential target for therapeutical applications, because its activity is rather low in tumor cells. It has been shown that NMNAT1 can inhibit recombinant human poly(ADP-ribose) polymerase-1 (PARP-1) by about 35% and completely prevent the formation of branched ADP-ribose polymers.

製品内容

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出荷温度及び保存条件

出荷温度
Dry Ice
短期保存温度
-80°C
長期保存温度
-80°C
保管に関する情報
-80°C

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

Nmnat1 also known as nicotinamide mononucleotide adenylyltransferase 1 is an enzyme involved in the conversion of nicotinamide mononucleotide (NMN) to nicotinamide adenine dinucleotide (NAD+). This enzyme weighs approximately 32 kDa and is expressed largely in mammalian tissues with higher concentrations in the brain heart and liver. In the research community variations like 'nmn ireland' or 'elisa namn' may refer to the study tools or location of research related to NMNAT.
Biological function summary

NMNAT1 plays a role in NAD+ biosynthesis which is essential for energy metabolism and cellular functions. It acts as a NAD+ synthase and may not work alone but within larger enzymatic complexes that handle cellular redox reactions. In neurons the enzyme supports axonal survival which connects it to neurodegenerative health studies.

Pathways

This enzyme becomes critical in the NAD+ biosynthesis pathway interacting closely with proteins such as nicotinamide phosphoribosyltransferase (NAMPT) in the salvage pathway. This pathway is key in maintaining cellular energy balance and gene expression regulation. The enzyme along with these related proteins ensures the recycling and regulation of NAD+ within the cells.

NMNAT1 holds significance in conditions like axonopathy and certain retinal degenerations. Mutations in the NMNAT1 gene have been linked to Leber's congenital amaurosis a severe genetic eye disorder. Studies often focus on NMNAT1 alongside other proteins like sirtuins as these participate in mitigating the oxidative stress aspects involved in neurodegeneration and associated disorders.

製品プロトコール

ターゲットの情報

Catalyzes the formation of NAD(+) from nicotinamide mononucleotide (NMN) and ATP (PubMed : 17402747). Can also use the deamidated form; nicotinic acid mononucleotide (NaMN) as substrate with the same efficiency (PubMed : 17402747). Can use triazofurin monophosphate (TrMP) as substrate (PubMed : 17402747). Also catalyzes the reverse reaction, i.e. the pyrophosphorolytic cleavage of NAD(+) (PubMed : 17402747). For the pyrophosphorolytic activity, prefers NAD(+) and NaAD as substrates and degrades NADH, nicotinic acid adenine dinucleotide phosphate (NHD) and nicotinamide guanine dinucleotide (NGD) less effectively (PubMed : 17402747). Involved in the synthesis of ATP in the nucleus, together with PARP1, PARG and NUDT5 (PubMed : 27257257). Nuclear ATP generation is required for extensive chromatin remodeling events that are energy-consuming (PubMed : 27257257). Also acts as a cofactor for glutamate and aspartate ADP-ribosylation by directing PARP1 catalytic activity to glutamate and aspartate residues on histones (By similarity). Fails to cleave phosphorylated dinucleotides NADP(+), NADPH and NaADP(+) (PubMed : 17402747). Protects against axonal degeneration following mechanical or toxic insults (By similarity). Neural protection does not correlate with cellular NAD(+) levels but may still require enzyme activity (By similarity).
See full target information NMNAT1

文献 (1)

Recent publications for all applications. Explore the full list and refine your search

Science advances 11:eadr8648 PubMed40106551

2025

PPDPF preserves integrity of proximal tubule by modulating NMNAT activity in chronic kidney diseases.

Applications

Unspecified application

Species

Unspecified reactive species

Xiaoliang Fang,Yi Zhong,Rui Zheng,Qihui Wu,Yu Liu,Dexin Zhang,Yuwei Wang,Wubing Ding,Kaiyuan Wang,Fengbo Zhong,Kai Lin,Xiaohui Yao,Qingxun Hu,Xiaofei Li,Guofeng Xu,Na Liu,Jing Nie,Dali Li,Hongquan Geng,Yuting Guan
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