CWF19L1 抗体 (Biotin)
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- 抗原 See all CWF19L1 products
- CWF19L1 (CWF19-Like 1, Cell Cycle Control (CWF19L1))
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适用
- 人, 大鼠, 小鼠
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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 CWF19L1 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CWF19L1
- 亚型
- IgG
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anti-CWF19-Like 1, Cell Cycle Control (CWF19L1) (AA 101-330) antibody
CWF19L1 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 - 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
- CWF19L1 (CWF19-Like 1, Cell Cycle Control (CWF19L1))
- 别名
- CWF19L1 (CWF19L1 产品)
- 别名
- 2610528C06Rik antibody, AI854304 antibody, AV336991 antibody, CWF19-like 1, cell cycle control (S. pombe) antibody, CWF19 like 1, cell cycle control (S. pombe) antibody, CWF19 like 1, cell cycle control (S. pombe) L homeolog antibody, Cwf19l1 antibody, CWF19L1 antibody, cwf19l1.L antibody
- 背景
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Synonyms: CWF19-like 1, cell cycle control, C19L1_HUMAN.
Background: CWF19L1 is a 538 amino acid protein belonging to the CWF19 family and exists as three alternatively spliced isoforms. CWF19L1 is encoded by a gene located on human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
- 基因ID
- 55280
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