C7ORF57 抗体 (AA 161-260) (HRP)
Our Local Distributor
北京 101111
Quick Overview for C7ORF57 抗体 (AA 161-260) (HRP) (ABIN1711862)
抗原
适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 161-260
-
交叉反应
- 大鼠
-
预测反应
- Human,Mouse,Cow,Sheep,Horse
-
纯化方法
- Purified by Protein A.
-
免疫原
- KLH conjugated synthetic peptide derived from human C7orf57
-
亚型
- IgG
-
-
anti-Chromosome 7 Open Reading Frame 57 (C7ORF57) (AA 161-260) antibody
C7ORF57 适用: 大鼠 IF (cc), IF (p), ELISA, IHC (fro), IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
-
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
-
-
- C7ORF57 (Chromosome 7 Open Reading Frame 57 (C7ORF57))
-
别名
- C7orf57
-
背景
-
Synonyms: C7orf57, CG057_HUMAN, Chromosome 7 open reading frame 57, Uncharacterized protein C7orf57.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.
-
基因ID
- 136288
-
UniProt
- Q8NEG2
抗原
-
