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NAT6/FUS2 Polyclonal antibody

NAT6/FUS2 Polyclonal Antibody for WB, IF/ICC, ELISA
Cat No. 15476-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

WB, IF/ICC, ELISA and More (1)

NAA80, NAT6, N-acetyltransferase 6, HsNAAA80, FUS2

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -


经过测试的应用

Positive WB detected inHeLa cells
Positive IF/ICC detected inHeLa cells

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:500-1:2000
Immunofluorescence (IF)/ICCIF/ICC : 1:200-1:800
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.

产品信息

15476-1-AP targets NAT6/FUS2 in WB, IF/ICC, ELISA applications and shows reactivity with human samples.

经测试应用 WB, IF/ICC, ELISA Application Description
文献引用应用WB, IF
经测试反应性 human
文献引用反应性human
免疫原 NAT6/FUS2 fusion protein Ag7780 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 N-acetyltransferase 6 (GCN5-related)
别名 NAA80, NAT6, N-acetyltransferase 6, HsNAAA80, FUS2
计算分子量 31 kDa
观测分子量45 kDa
GenBank蛋白编号BC004483
基因名称 FUS2
Gene ID (NCBI) 24142
RRIDAB_3085463
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ93015
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

The acetyltransferase NAT6 (also known as Fus2) is an enzyme that catalyzes the transfer of acetyl groups from acetyl-CoA to acrylamines and located mainly in the cytoplasm. NAT6 has two isoforms. The molecular weight of NAT6 was detected to be about 45kDa (PMID:32978259).

实验方案

Product Specific Protocols
WB protocol for NAT6/FUS2 antibody 15476-1-APDownload protocol
IF protocol for NAT6/FUS2 antibody 15476-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
humanWB,IF

FEBS J

NAT6 acetylates the N-terminus of different forms of actin.

Authors - Elsa Wiame
  • KO Validated
humanWB

Brain Commun

NAA80 bi-allelic missense variants result in high-frequency hearing loss, muscle weakness and developmental delay.

Authors - Irena J J Muffels
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