C3orf24 抗体 (FITC)
-
- 抗原 See all C3orf24 抗体
- C3orf24 (Chromosome 3 Open Reading Frame 24 (C3orf24))
-
适用
- 人, 大鼠, 小鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C3orf24 antibody is conjugated to FITC
-
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 C3orf24
- 亚型
- IgG
- Top Product
- Discover our top product C3orf24 Primary Antibody
-
anti-Chromosome 3 Open Reading Frame 24 (C3orf24) (AA 71-120) antibody
C3orf24 适用: 人, 大鼠, 小鼠, 马, 兔, 豚鼠, Cow, 犬, Bat, Pig, 猴, Hamster WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
- IF(IHC-P) 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
- C3orf24 (Chromosome 3 Open Reading Frame 24 (C3orf24))
- 别名
- C3orf24 (C3orf24 产品)
- 别名
- C3orf24 antibody, RGD1565997 antibody, FANCD2 opposite strand L homeolog antibody, FANCD2 opposite strand antibody, fancd2os.L antibody, FANCD2OS antibody, fancd2os antibody, Fancd2os antibody
- 背景
-
Synonyms: C3orf24, CC024_HUMAN, chromosome 3 open reading frame 24, HSD19, hypothetical protein LOC115795, MGC40179, Uncharacterized protein C3orf24.
Background: C3orf24, also known as MGC40179, is a 177 amino acid protein that is encoded by a gene that maps to human chromosome 3p25.3. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.
- 基因ID
- 115795
-
