CCDC148 抗体 (AA 401-500) (Alexa Fluor 594)
-
- 抗原 See all CCDC148 抗体
- CCDC148 (Coiled-Coil Domain Containing 148 (CCDC148))
-
抗原表位
- AA 401-500
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This CCDC148 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,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CCDC148
- 亚型
- IgG
- Top Product
- Discover our top product CCDC148 Primary Antibody
-
anti-Coiled-Coil Domain Containing 148 (CCDC148) (AA 1-255) antibody
CCDC148 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 148 (CCDC148) (AA 279-307) antibodyCCDC148 适用: 人, 小鼠 WB, FACS 宿主: 兔 Polyclonal RB28328 unconjugated
anti-Coiled-Coil Domain Containing 148 (CCDC148) (AA 286-316), (Middle Region) antibodyCCDC148 适用: 人, 小鼠 WB, FACS, EIA 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
- CCDC148 (Coiled-Coil Domain Containing 148 (CCDC148))
- 别名
- CCDC148 (CCDC148 产品)
- 别名
- 5830402J09 antibody, RGD1561169 antibody, coiled-coil domain containing 148 antibody, CCDC148 antibody, Ccdc148 antibody
- 背景
-
Synonyms: CCDC 148, coiled coil domain containing 148, coiled-coil domain containing 148, CC148_HUMAN.
Background: CCDC148 (coiled-coil domain containing 148), also known as MGC125590 or MGC125588, is a 591 amino acid protein encoded by a gene mapping to human chromosome 2. The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.
-
