PHF6 抗体 (AA 37-309)
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Quick Overview for PHF6 抗体 (AA 37-309) (ABIN7874395)
抗原
See all PHF6 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 37-309
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原理
- PHF6 Antibody / PHD finger protein 6
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纯化方法
- Antigen affinity chromatography
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免疫原
- An E.coli-derived human recombinant protein (amino acids Q37-D309) was used as the immunogen for the PHF6 antibody.
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亚型
- IgG
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anti-PHD Finger Protein 6 (PHF6) (AA 2-312) antibody
PHF6 适用: 人 WB, ELISA, IHC, IP, IF 宿主: 兔 Polyclonal unconjugated
anti-PHD Finger Protein 6 (PHF6) (AA 125-175) antibodyPHF6 适用: 人, 小鼠 IHC, IF (p) 宿主: 兔 Polyclonal unconjugated
anti-PHD Finger Protein 6 (PHF6) antibodyPHF6 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-PHD Finger Protein 6 (PHF6) (AA 315-349) antibodyPHF6 适用: 人 WB, IF 宿主: 兔 Polyclonal RB54601 unconjugated
anti-PHD Finger Protein 6 (PHF6) (AA 1-312) antibodyPHF6 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-PHD Finger Protein 6 (PHF6) (AA 1-99) antibodyPHF6 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 8F24 unconjugated
anti-PHD Finger Protein 6 (PHF6) (AA 125-175) antibodyPHF6 适用: 人 WB, IP, IHC (fp) 宿主: 兔 Polyclonal unconjugated
anti-PHD Finger Protein 6 (PHF6) (Isoform 1), (N-Term) antibodyPHF6 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-PHD Finger Protein 6 (PHF6) (AA 148-180) antibodyPHF6 适用: 人 WB 宿主: 兔 Polyclonal RB54600 unconjugated
anti-PHD Finger Protein 6 (PHF6) (Middle Region) antibodyPHF6 适用: 人, 小鼠, 犬, Cow, 大鼠, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the PHF6 antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the PHF6 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- PHF6 (PHD Finger Protein 6 (PHF6))
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别名
- PHF6
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背景
- PHD finger protein 6 is a protein that in humans is encoded by the PHF6 gene. This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms.
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UniProt
- Q8IWS0
抗原
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