CCDC25 抗体 (AA 71-170) (Alexa Fluor 594)
-
- 抗原 See all CCDC25 抗体
- CCDC25 (Coiled-Coil Domain Containing 25 (CCDC25))
-
抗原表位
- AA 71-170
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This CCDC25 antibody is conjugated to Alexa Fluor 594
-
应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC25
- 亚型
- IgG
- Top Product
- Discover our top product CCDC25 Primary Antibody
-
anti-Coiled-Coil Domain Containing 25 (CCDC25) (C-Term) antibody
CCDC25 适用: 人, 小鼠, 大鼠, 马, 兔, 斑马鱼, Bat, 猴, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - 限制
- 仅限研究用
-
- 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
-
- 抗原
- CCDC25 (Coiled-Coil Domain Containing 25 (CCDC25))
- 别名
- CCDC25 (CCDC25 产品)
- 背景
-
Synonyms: CCD25_HUMAN, CCDC25, coiled-coil domain containing 25, CCDC25 coiled coil domain containing 25.
Background: CCDC25 is a 208 amino acid protein encoded by a gene that maps to human chromosome 8p21.1. 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.
- 基因ID
- 55246
-
