TBL1XR1 Protein (His tag)
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- 抗原 See all TBL1XR1 蛋白
- TBL1XR1 (Transducin (Beta)-Like 1 X-Linked Receptor 1 (TBL1XR1))
- 蛋白类型
- Recombinant
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宿主
- 人
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资源
- 大肠杆菌(E. Coli)
- 标记
- This TBL1XR1 protein is labelled with His tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human TBL1XR1 (full length, N-term HIS tag) protein expressed in E.coli.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product TBL1XR1 蛋白
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- 应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 说明
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The tag is located at the N-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- 抗原
- TBL1XR1 (Transducin (Beta)-Like 1 X-Linked Receptor 1 (TBL1XR1))
- 别名
- Tbl1xr1 (TBL1XR1 产品)
- 别名
- tbl1xr1 Protein, zgc:63617 Protein, c21 Protein, dc42 Protein, ira1 Protein, TBLR1 Protein, TBL1XR1 Protein, wu:fc46g07 Protein, zgc:110312 Protein, C21 Protein, DC42 Protein, IRA1 Protein, RGD1560053 Protein, 8030499H02Rik Protein, A630076E03Rik Protein, AW539987 Protein, C230089I12Rik Protein, Ira1 Protein, transducin (beta)-like 1 X-linked receptor 1b Protein, transducin (beta)-like 1 X-linked receptor 1 Protein, transducin (beta)-like 1 X-linked receptor 1a Protein, transducin beta like 1 X-linked receptor 1 Protein, transducin (beta)-like 1X-linked receptor 1 Protein, tbl1xr1b Protein, tbl1xr1 Protein, tbl1xr1a Protein, TBL1XR1 Protein, Tbl1xr1 Protein
- 背景
- This gene is a member of the WD40 repeat-containing gene family and shares sequence similarity with transducin (beta)-like 1X-linked (TBL1X). The protein encoded by this gene is thought to be a component of both nuclear receptor corepressor (N-CoR) and histone deacetylase 3 (HDAC 3) complexes, and is required for transcriptional activation by a variety of transcription factors. Mutations in these gene have been associated with some autism spectrum disorders, and one finding suggests that haploinsufficiency of this gene may be a cause of intellectual disability with dysmorphism. Mutations in this gene as well as recurrent translocations involving this gene have also been observed in some tumors.
- 分子量
- 55.4 kDa
- NCBI登录号
- NP_078941
- 途径
- Regulation of Lipid Metabolism by PPARalpha
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