C1orf55 抗体 (AA 51-150) (Cy5)
-
- 抗原 See all C1orf55 products
- C1orf55 (Chromosome 1 Open Reading Frame 55 (C1orf55))
-
抗原表位
- AA 51-150
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C1orf55 antibody is conjugated to Cy5
-
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,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C1orf55
- 亚型
- IgG
-
anti-Chromosome 1 Open Reading Frame 55 (C1orf55) (C-Term) antibody
C1orf55 适用: 人, 小鼠, 大鼠, 犬, Cow, 斑马鱼, 豚鼠, 马, 猴, Bat, 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
- C1orf55 (Chromosome 1 Open Reading Frame 55 (C1orf55))
- 别名
- C1orf55 (C1orf55 产品)
- 别名
- C1orf55 antibody, RP4-671D7.1 antibody, dJ671D7.1 antibody, SDE2 antibody, c1orf55 antibody, DKFZp469F1217 antibody, RGD1305572 antibody, wu:fb55e02 antibody, wu:fi34c02 antibody, zgc:112095 antibody, SDE2 telomere maintenance homolog antibody, SDE2 telomere maintenance homolog (S. pombe) S homeolog antibody, SDE2 telomere maintenance homolog (S. pombe) antibody, SDE2 antibody, sde2.S antibody, sde2 antibody, Sde2 antibody
- 背景
-
Synonyms: C1orf55, CA055_HUMAN, Chromosome 1 open reading frame 55, dJ671D7.1, FLJ35382, Hypothetical protein LOC163859, RP4 671D7.1, UPF0667 protein C1orf55.
Background: Belonging to the UPF0667 family, C1orf55 is a 451 amino acid protein that is phosphorylated upon DNA damage, likely by Atm or ATR. There are three different isoforms of C1orf55 that are produced as a result of alternative splicing events. The gene encoding C1orf55 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.
- 基因ID
- 163859
-
