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AB60065

Anti-NARG1抗体[434C2a]

Anti-NARG1 antibody [434C2a]

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(3 Publications)

Mouse Monoclonal NARG1 antibody. Suitable for WB and reacts with Recombinant fragment samples. Cited in 3 publications. Immunogen corresponding to Recombinant Fragment Protein within Human NAA15.

查看别名

GA19, NARG1, NATH, TBDN100, NAA15, Gastric cancer antigen Ga19, N-terminal acetyltransferase, NMDA receptor-regulated protein 1, Protein tubedown-1, Tbdn100

1 Images
Western blot - Anti-NARG1 antibody [434C2a] (AB60065)
  • WB

Unknown

Western blot - Anti-NARG1 antibody [434C2a] (AB60065)

Western blot analysis of immunized recombinant protein, using ab60065

All lanes:

Western blot - Anti-NARG1 antibody [434C2a] (ab60065)

Predicted band size: 101 kDa

Observed band size: 32 kDa

false

关键信息

宿主种属

Mouse

克隆

Monoclonal

克隆号

434C2a

亚型

IgG1

不含载体蛋白

No

应用

WB

applications

免疫原

Recombinant Fragment Protein within Human NAA15. The exact immunogen used to generate this antibody is proprietary information.

Q9BXJ9

反应性数据

{ "title": "Reactivity Data", "filters": { "stats": ["", "Species", "Dilution Info", "Notes"], "tabs": { "all-applications": {"fullname" : "All Applications", "shortname": "All Applications"}, "WB" : {"fullname" : "Western blot", "shortname":"WB"} }, "product-promise": { "all": "all", "testedAndGuaranteed": "tested", "guaranteed": "expected", "predicted": "predicted", "notRecommended": "not-recommended" } }, "values": { "Recombinant fragment": { "WB-species-checked": "testedAndGuaranteed", "WB-species-dilution-info": "", "WB-species-notes": "<p></p>" } } }

性能和储存信息

形式
Liquid
纯化工艺
Affinity purification Protein G
纯化说明
Purified using protein G column chromatography, from culture supernatant of hybridoma cultured in a medium containing bovine IgG-depleted (approximately 95%) fetal bovine serum.
存储溶液
pH: 7.4 Preservative: 0.05% Sodium azide Constituents: PBS, 1% BSA, 0.812% Sodium chloride, 0.1312% Sodium phosphate, 0.03% Tripotassium orthophosphate, 0.0225% Potassium chloride
运输条件
Blue Ice
推荐的短期储存条件
+4°C
推荐的长期储存条件
-20°C
分装信息
Upon delivery aliquot
储存信息
Avoid freeze / thaw cycle

补充信息

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

NARG1 also known as NARGG or NMDA receptor-regulated gene protein 1 is a protein with a molecular mass of approximately 152 kDa. NARG1 directly participates in protein acetylation by transferring acetyl groups to lysine residues an important post-translational modification affecting protein function and interactions. This protein is expressed across various tissues with notable presence in the brain heart and testis indicating its diverse functional roles within different physiological contexts.
Biological function summary

The acetyltransferase activity of NARG1 significantly impacts gene regulation and cellular homeostasis. It forms part of the NatA complex where it functions together with other components such as NAA10 and NAA15. This complex plays a role in co-translational N-terminal acetylation influencing protein stability and function. NARG1's activity particulary affects processes like cell cycle progression apoptosis and cellular differentiation reflecting its importance in maintaining cellular balance.

Pathways

NARG1 activity links prominently to the signaling pathway of mRNA translation which is essential for protein synthesis and cellular growth. Additionally it participates in the regulation of apoptosis pathways modulating cell survival in response to various stress signals. Proteins like p53 and BCL-2 show interactions with these pathways revealing how NARG1 may influence key cellular outcomes and decision points regarding survival and death.

Studies have connected NARG1 to neural development and certain neurodegenerative conditions. Aberrations in NARG1 expression or function may contribute to disorders like Alzheimer’s Disease potentially affecting neuronal survival and cognitive function. The protein's role is also noteworthy in the context of cardiac hypertrophy where its regulatory capacity on cellular growth pathways can impact heart muscle function. Related proteins affected by these conditions may include components like tau in neurodegeneration and myosin heavy chain in cardiac pathophysiology.

产品实验方案

For this product, it's our understanding that no specific protocols are required. You can visit:

靶点信息

Auxillary subunit of N-terminal acetyltransferase complexes which display alpha (N-terminal) acetyltransferase (NAT) activity (PubMed : 15496142, PubMed : 20154145, PubMed : 29754825, PubMed : 32042062). The NAT activity may be important for vascular, hematopoietic and neuronal growth and development (PubMed : 15496142). Required to control retinal neovascularization in adult ocular endothelial cells (PubMed : 11687548). In complex with XRCC6 and XRCC5 (Ku80), up-regulates transcription from the osteocalcin promoter (PubMed : 12145306).
See full target information NAA15

文献 (3)

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

Experimental cell research 414:113083 PubMed35227662

2022

Evidence that the transcriptional repressor ICER is regulated via the N-end rule for ubiquitination.

Applications

Unspecified application

Species

Unspecified reactive species

Angelo Cirinelli,Justin Wheelan,Christopher Grieg,Carlos A Molina

eLife 10: PubMed34355692

2021

compensates for in mice in the amino-terminal acetylation pathway.

Applications

Unspecified application

Species

Unspecified reactive species

Hyae Yon Kweon,Mi-Ni Lee,Max Dorfel,Seungwoon Seo,Leah Gottlieb,Thomas PaPazyan,Nina McTiernan,Rasmus Ree,David Bolton,Andrew Garcia,Michael Flory,Jonathan Crain,Alison Sebold,Scott Lyons,Ahmed Ismail,Elaine Marchi,Seong-Keun Sonn,Se-Jin Jeong,Sejin Jeon,Shinyeong Ju,Simon J Conway,Taesoo Kim,Hyun-Seok Kim,Cheolju Lee,Tae-Young Roh,Thomas Arnesen,Ronen Marmorstein,Goo Taeg Oh,Gholson J Lyon

Yeast (Chichester, England) 34:19-37 PubMed27668839

2016

Proteomic and genomic characterization of a yeast model for Ogden syndrome.

Applications

WB

Species

Unspecified reactive species

Max J Dörfel,Han Fang,Jonathan Crain,Michael Klingener,Jake Weiser,Gholson J Lyon
View all publications

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