SKIDA1 抗体 (AbBy Fluor® 555)
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- 抗原 See all SKIDA1 products
- SKIDA1 (SKI/DACH Domain Containing 1 (SKIDA1))
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适用
- 人, 小鼠, 大鼠
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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 SKIDA1 antibody is conjugated to AbBy Fluor® 555
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (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 C10orf140
- 亚型
- IgG
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anti-SKI/DACH Domain Containing 1 (SKIDA1) (AA 772-821) antibody
SKIDA1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 1:50-200
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- SKIDA1 (SKI/DACH Domain Containing 1 (SKIDA1))
- 别名
- C10orf140 (SKIDA1 产品)
- 别名
- C10orf140 antibody, DLN-1 antibody, 2810030E01Rik antibody, 5730507N06Rik antibody, BB088113 antibody, SKI/DACH domain containing 1 antibody, SKIDA1 antibody, Skida1 antibody
- 背景
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Synonyms: C10orf140, chromosome 10 open reading frame 140, DKFZp761J229, DLN 1, DLN1_HUMAN, FLJ45187, Protein DLN-1.
Background: C10orf140, also known as DLN-1, is an 827 amino acid protein that belongs to the DACH/dachshund family. C10orf140 contains a poly-Alanine region that is highly polymorphic. The gene encoding C10orf140 maps to 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
- 387640
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