NMNAT1 Polyclonal antibody

NMNAT1 Polyclonal Antibody for WB, ELISA
Cat No. 28493-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

Human, mouse and More (1)

应用

WB, ELISA

NaMN adenylyltransferase 1, NMNAT1, PNAT 1, PNAT1

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格价格库存


经过测试的应用

Positive WB detected inmouse skeletal muscle tissue
Planning an IHC experiment? We recommend our IHCeasy NMNAT1 Ready-To-Use IHC Kit. NMNAT1 primary antibody included.

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:500-1:2000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

发表文章中的应用

WBSee 1 publications below

产品信息

28493-1-AP targets NMNAT1 in WB, ELISA applications and shows reactivity with Human, mouse samples.

经测试应用 WB, ELISA Application Description
文献引用应用WB
经测试反应性 Human, mouse
文献引用反应性human, mouse
免疫原

CatNo: Ag29584

Product name: Recombinant human NMNAT1 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 52-152 aa of BC014943

Sequence: GDAYKKKGLIPAYHRVIMAELATKNSKWVEVDTWESLQKEWKETLKVLRHHQEKLEASDCDHQQNSPTLERPGRKRKWTETQDSSQKKSLEPKTKAVPKVK

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 nicotinamide nucleotide adenylyltransferase 1
别名 NaMN adenylyltransferase 1, NMNAT1, PNAT 1, PNAT1
计算分子量 33 kDa
观测分子量 35 kDa
GenBank蛋白编号BC014943
基因名称 NMNAT1
Gene ID (NCBI) 64802
RRIDAB_3086056
偶联类型 Unconjugated
形式Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ9HAN9
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

NMNAT1 is a member of the nicotinamide-nucleotide adenylyltransferases (NMNATs) which catalyze nicotinamide adenine dinucleotide (NAD) synthesis (PMID: 28445802). NMNAT is a central enzyme in NAD biosynthesis, catalyzing the formation of NAD+ from nicotinamide mononucleotide (NMN) and ATP (PMID: 17402747). NMNAT1 is widely expressed with the highest levels in skeletal muscle, heart, and kidney(PMID: 11027696). Mutations in NMNAT1 have been shown associated with the LCA9 form of the retinal degeneration pathology Leber's congenital amaurosis (PMID: 22842229, 22842230).

实验方案

Product Specific Protocols
WB protocol for NMNAT1 antibody 28493-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
human,mouseWB

Nat Cardiovasc Res

Mitochondrial NAD+ deficiency in vascular smooth muscle impairs collagen III turnover to trigger thoracic and abdominal aortic aneurysm

Authors - Jingjing Zhang
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