GTF2IRD2B 抗体 (C-Term)
This anti-GTF2IRD2B antibody is a 兔 多克隆 antibody detecting GTF2IRD2B in WB. Suitable for 人. This Primary Antibody has been cited in 2+ publications.
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(2 references)Quick Overview for GTF2IRD2B 抗体 (C-Term) (ABIN1881397)
抗原
See all GTF2IRD2B 抗体
GTF2IRD2B
(GTF2I Repeat Domain Containing 2B (GTF2IRD2B))
适用
人
宿主
兔
克隆类型
多克隆
标记
This GTF2IRD2B antibody is un-conjugated
应用范围
Western Blotting (WB)
克隆位点
RB40709
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抗原表位
- AA 467-494, C-Term
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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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.
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亚型
- Ig Fraction
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应用备注
- WB: 1:1000
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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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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- GTF2IRD2B (GTF2I Repeat Domain Containing 2B (GTF2IRD2B))
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别名
- GTF2IRD2B
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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.
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分子量
- 107233
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NCBI登录号
- NP_001003795
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UniProt
- Q6EKJ0
抗原
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