PHF21B 抗体 (AA 291-499)
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北京 101111
Quick Overview for PHF21B 抗体 (AA 291-499) (ABIN7601150)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 291-499
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原理
- Anti-PHF21B Antibody
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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产品特性
- Anti-PHF21B Antibody (ABIN7601150). Tested in ELISA, IF, ICC, WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human PHF21B recombinant protein (Position: E291-M499).
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亚型
- IgG
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anti-PHD Finger Protein 21B (PHF21B) (AA 322-531) antibody
PHF21B 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-PHD Finger Protein 21B (PHF21B) (AA 1-531) antibodyPHF21B 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-PHD Finger Protein 21B (PHF21B) antibodyPHF21B 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
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Western blot, 0.25-0.5 μg/mL, Human
Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
ELISA, 0.1-0.5 μg/mL, -
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限制
- 仅限研究用
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状态
- Lyophilized
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溶解方式
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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浓度
- 500 μg/mL
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缓冲液
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.
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储存条件
- 4 °C,-20 °C
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储存方法
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
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- PHF21B (PHD Finger Protein 21B (PHF21B))
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别名
- PHF21B
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背景
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Synonyms: Kelch repeat and BTB domain-containing protein 2, BTB and kelch domain-containing protein 1, KBTBD2, BKLHD1, KIAA1489
Tissue Specificity: Detected in liver, skeletal muscle, kidney, pancreas, spleen, thyroid, testis, ovary, small intestine and colon.
Background: PHF21B (PHD finger protein 21B), also known as PHF4, is a 531 amino acid protein that contains one PHD-type zinc finger and is expressed as multiple alternatively spliced isoforms. The gene encoding PHF21B maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia.
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分子量
- 57 kDa
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基因ID
- 112885
抗原
-
