C11orf65 抗体 (FITC)
-
- 抗原 See all C11orf65 products
- C11orf65 (Chromosome 11 Open Reading Frame 65 (C11orf65))
-
适用
- 人, 大鼠, 小鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C11orf65 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 C11orf65
- 亚型
- IgG
-
anti-Chromosome 11 Open Reading Frame 65 (C11orf65) (N-Term) antibody
C11orf65 适用: 人, 大鼠, 小鼠, 马, Pig, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 11 Open Reading Frame 65 (C11orf65) (N-Term) antibodyC11orf65 适用: 人, 大鼠, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 11 Open Reading Frame 65 (C11orf65) (N-Term) antibodyC11orf65 适用: 人, 大鼠, 小鼠, 马, 豚鼠, 兔 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
- C11orf65 (Chromosome 11 Open Reading Frame 65 (C11orf65))
- 别名
- C11orf65 (C11orf65 产品)
- 别名
- AU017961 antibody, chromosome 11 open reading frame 65 antibody, chromosome 11 open reading frame 65 L homeolog antibody, chromosome 14 open reading frame, human C11orf65 antibody, RIKEN cDNA 4930550C14 gene antibody, similar to RIKEN cDNA 4930550C14 antibody, C11orf65 antibody, c11orf65.L antibody, C14H11orf65 antibody, 4930550C14Rik antibody, RGD1311251 antibody
- 背景
-
Synonyms: Chromosome 11 open reading frame 65, Hypothetical protein LOC160140, CK065_HUMAN.
Background: C11orf65, also known as MGC33948, is a 313 amino acid protein that 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
- 160140
-
