验证数据展示
经过测试的应用
Positive WB detected in | mouse ovary tissue |
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
WB | See 1 publications below |
IHC | See 1 publications below |
产品信息
12094-1-AP targets DDIT4L in WB, IHC, ELISA applications and shows reactivity with mouse samples.
经测试应用 | WB, ELISA Application Description |
文献引用应用 | WB, IHC |
经测试反应性 | mouse |
文献引用反应性 | mouse |
免疫原 | DDIT4L fusion protein Ag2735 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 | DNA-damage-inducible transcript 4-like |
别名 | DNA damage-inducible transcript 4-like protein, HIF-1 responsive protein RTP801-like, REDD2, REDD-2, RTP801L |
计算分子量 | 193 aa, 22 kDa |
观测分子量 | 22 kDa |
GenBank蛋白编号 | BC013592 |
基因名称 | DDIT4L |
Gene ID (NCBI) | 115265 |
RRID | AB_2918027 |
偶联类型 | Unconjugated |
形式 | Liquid |
纯化方式 | Antigen affinity purification |
UNIPROT ID | Q96D03 |
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
DNA-damage-inducible transcript 4-like protein(DDIT4L), encoded by the stress responsive gene REDD2, is a negative regulator of mTOR signaling, and expressed predominantly in skeletal muscle. It regulates the TOR signaling pathway upstream of the TSC1-TSC2 complex and downstream of AKT1. Also, DDIT4L involves in oxidized low-density lipoprotein-induced macrophage death sensitivity.
实验方案
Product Specific Protocols | |
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WB protocol for DDIT4L antibody 12094-1-AP | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |
发表文章
Species | Application | Title |
---|---|---|
J Cell Sci Oocyte-dependent activation of MTOR in cumulus cells controls the development and survival of cumulus-oocyte complexes. | ||
Am J Physiol Endocrinol Metab Disruption of REDD1 gene ameliorates sepsis-induced decrease in mTORC1 signaling but has divergent effects on proteolytic signaling in skeletal muscle. |