FAM203B 抗体
Quick Overview for FAM203B 抗体 (ABIN7244606)
抗原
适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Antigen affinity purification
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免疫原
- Synthetic peptide of human HGH1
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亚型
- IgG
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anti-Family with Sequence Similarity 203, Member B (FAM203B) (Internal Region) antibody
FAM203B 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 203, Member B (FAM203B) (AA 1-390) antibodyFAM203B 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Family with Sequence Similarity 203, Member B (FAM203B) (Internal Region) antibodyFAM203B 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 203, Member B (FAM203B) (AA 254-280) antibodyFAM203B 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB38155 unconjugated
anti-Family with Sequence Similarity 203, Member B (FAM203B) antibodyFAM203B 适用: 人, 猴 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 203, Member B (FAM203B) (AA 251-300) antibodyFAM203B 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC 1:30-1:150, ELISA 1:5000-1:10000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.6 mg/mL
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缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- FAM203B (Family with Sequence Similarity 203, Member B (FAM203B))
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别名
- HGH1
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背景
- HGH1, is also known as BRP16, Brp16 is a 256 amino acid protein encoded by a gene on human chromosome 8. Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.
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UniProt
- Q9BTY7
抗原
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