C1orf122 抗体 (AA 11-80) (HRP)
-
- 抗原 See all C1orf122 products
- C1orf122 (Chromosome 1 Open Reading Frame 122 (C1orf122))
-
抗原表位
- AA 11-80
- 适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This C1orf122 antibody is conjugated to HRP
-
应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C1orf122
- 亚型
- IgG
-
anti-Chromosome 1 Open Reading Frame 122 (C1orf122) (N-Term) antibody
C1orf122 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 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.
- 注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- 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
- C1orf122 (Chromosome 1 Open Reading Frame 122 (C1orf122))
- 别名
- C1orf122 (C1orf122 产品)
- 别名
- ALAESM antibody, chromosome 1 open reading frame 122 antibody, C1orf122 antibody
- 背景
-
Synonyms: ALAESM, Chromosome 1 open reading frame 122, FLJ23476, FLJ45459, Hypothetical protein LOC127687, Protein ALAESM, Uncharacterized protein C1orf122,CA122_HUMAN.
Background: Chromosome 1 is 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. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf122 gene product has been provisionally designated C1orf122 pending further characterization.
- 基因ID
- 127687
-
