GTF2IRD2 抗体 (full length)
The 小鼠 单克隆 anti-GTF2IRD2 antibody (Clone PCRP-GTF2IRD2-1B12) (ABIN7878331) specifically detects GTF2IRD2 in WB 和 FACS.
The antibody is reactive with 人 samples.
产品编号 ABIN7878331
发货至:
中国
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Quick Overview for GTF2IRD2 抗体 (full length) (ABIN7878331)
抗原
See all GTF2IRD2 抗体
GTF2IRD2
(GTF2I Repeat Domain Containing 2 (GTF2IRD2))
适用
人
宿主
小鼠
克隆类型
单克隆
标记
This GTF2IRD2 antibody is un-conjugated
应用范围
Western Blotting (WB), Flow Cytometry (FACS)
克隆位点
PCRP-GTF2IRD2-1B12
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抗原表位
- full length
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原理
- GTF2IRD2 alpha Antibody / GTF2IRD2
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纯化方法
- Protein A/G affinity
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免疫原
- Recombinant full-length human General transcription factor II-I repeat domain-containing protein 2A protein was used as the immunogen for the GTF2IRD2 alpha antibody.
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亚型
- IgG2b
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anti-GTF2I Repeat Domain Containing 2 (GTF2IRD2) (AA 1-498) antibody
GTF2IRD2 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-GTF2I Repeat Domain Containing 2 (GTF2IRD2) (AA 812-841), (C-Term) antibodyGTF2IRD2 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB26073 unconjugated
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应用备注
- Optimal dilution of the GTF2IRD2 alpha antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.2 mg/mL
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缓冲液
- 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % 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
- -20 °C
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储存方法
- Aliquot the GTF2IRD2 alpha antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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- GTF2IRD2 (GTF2I Repeat Domain Containing 2 (GTF2IRD2))
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别名
- GTF2IRD2 alpha
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背景
- The TFII-I family contains two highly homologous 949 amino acid proteins, GTF2IRD2 (also called GTF2IRD2 alpha and GTF2IRD2A) and GTF2IRD2B. Localizing to the nucleus, these proteins are ubiquitously expressed and contain two GTF2I- like repeats. Encoded by a gene mapping to human chromosome 7q11.23, GTF2IRD2 and GTF2IRD2B are located in the Williams-Beuren syndrome (WBS) critical region. The deletion of genes located within this region results in WBS, possibly due to the unequal crossing over of highly homologous low-copy repeat sequences that flank the deleted region. WBS is an autosomal dominant genetic condition that is characterized by physical, cognitive and behavioral traits including facial dysmorphology, vascular stenoses, growth deficiencies, dental anomalies and neurologic and musculoskeletal abnormalities.
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UniProt
- Q86UP8
抗原
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