GTF2IRD2B 抗体 (C-Term)
GTF2IRD2B
适用: 人
WB
宿主: 兔
Polyclonal
RB40709
unconjugated
1 image
(2 references)-
- 抗原 See all GTF2IRD2B 抗体
- GTF2IRD2B (GTF2I Repeat Domain Containing 2B (GTF2IRD2B))
- 抗原表位
- AA 467-494, C-Term
- 适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This GTF2IRD2B antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- 免疫原
- This GTF2IRD2B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 467-494 amino acids from the C-terminal region of human GTF2IRD2B.
- 克隆位点
- RB40709
- 亚型
- Ig Fraction
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- 应用备注
- WB: 1:1000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 有效期
- 6 months
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: "Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome." in: Protein science : a publication of the Protein Society, Vol. 13, Issue 10, pp. 2588-99, (2004) (PubMed).
: "Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome." in: European journal of human genetics : EJHG, Vol. 12, Issue 7, pp. 551-60, (2004) (PubMed).
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: "Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome." in: Protein science : a publication of the Protein Society, Vol. 13, Issue 10, pp. 2588-99, (2004) (PubMed).
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- 抗原
- GTF2IRD2B (GTF2I Repeat Domain Containing 2B (GTF2IRD2B))
- 别名
- GTF2IRD2B (GTF2IRD2B 产品)
- 别名
- GTF2I repeat domain containing 2B antibody, general transcription factor II-I repeat domain-containing protein 2B antibody, GTF2IRD2B antibody, LOC698860 antibody, gtf2ird2b antibody, LOC100607295 antibody
- 背景
- This gene encodes a glycosylated phosphoprotein with a leucine zipper motif, two helix-loop-helix motifs (I repeats) that are similar to domains found in the TFII-I family of transcription factors, one CHARLIE8 transposable element-like sequence, and a BED zinc finger. This gene lies within a region that is deleted in Williams-Beuren syndrome. Alternatively spliced variants which encode different protein isoforms have been described, however, not all variants have been fully characterized.
- 分子量
- 107233
- NCBI登录号
- NP_001003795
- UniProt
- Q6EKJ0
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