C11ORF74 抗体 (AbBy Fluor® 488)
-
- 抗原 See all C11ORF74 抗体
- C11ORF74 (Chromosome 11 Open Reading Frame 74 (C11ORF74))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C11ORF74 antibody is conjugated to AbBy Fluor® 488
-
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 C11orf74
- 亚型
- IgG
- Top Product
- Discover our top product C11ORF74 Primary Antibody
-
anti-Chromosome 11 Open Reading Frame 74 (C11ORF74) (C-Term) antibody
C11ORF74 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 11 Open Reading Frame 74 (C11ORF74) (AA 190-220), (C-Term) antibodyC11ORF74 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB27840 unconjugated
anti-Chromosome 11 Open Reading Frame 74 (C11ORF74) (AA 197-228), (C-Term) antibodyC11ORF74 适用: 人 WB, EIA 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
- C11ORF74 (Chromosome 11 Open Reading Frame 74 (C11ORF74))
- 别名
- C11orf74 (C11ORF74 产品)
- 别名
- HEPIS antibody, chromosome 11 open reading frame 74 antibody, chromosome 5 C11orf74 homolog antibody, C11orf74 antibody, C5H11orf74 antibody, c11orf74 antibody
- 背景
-
Synonyms: Chromosome 11 open reading frame 74, FLJ38678, HEPIS, Hypothetical protein LOC119710, Protein HEPIS, CK074_HUMAN.
Background: C11orf74, also known as FLJ38678, is a 123 amino acid protein that exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
- 基因ID
- 119710
-
