C8orf48 抗体 (AA 251-319) (Biotin)
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- 抗原 See all C8orf48 products
- C8orf48 (Chromosome 8 Open Reading Frame 48 (C8orf48))
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抗原表位
- AA 251-319
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This C8orf48 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C8orf48
- 亚型
- IgG
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anti-Chromosome 8 Open Reading Frame 48 (C8orf48) (AA 1-319) antibody
C8orf48 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- C8orf48 (Chromosome 8 Open Reading Frame 48 (C8orf48))
- 别名
- C8orf48 (C8orf48 产品)
- 别名
- chromosome 8 open reading frame 48 antibody, C8orf48 antibody
- 背景
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Synonyms: C8orf48, CH048_HUMAN, Chromosome 8 open reading frame 48, FLJ25402, Uncharacterized protein C8orf48.
Background: C8orf48 (chromosome 8 open reading frame 48) is a 319 amino acid protein encoded by a gene that maps to human chromosome 8p22. Consisting 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 are 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.
- 基因ID
- 157773
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