SMIM19 抗体 (AA 21-100) (Biotin)
-
- 抗原 See all SMIM19 products
- SMIM19 (Small Integral Membrane Protein 19 (SMIM19))
-
抗原表位
- AA 21-100
- 适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This SMIM19 antibody is conjugated to Biotin
-
应用范围
- ELISA, Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C8orf40
- 亚型
- IgG
-
anti-Small Integral Membrane Protein 19 (SMIM19) (AA 44-107) antibody
SMIM19 适用: 人 ELISA, IHC, IF 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.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
-
- 抗原
- SMIM19 (Small Integral Membrane Protein 19 (SMIM19))
- 别名
- C8orf40 (SMIM19 产品)
- 别名
- C8orf40 antibody, AI316807 antibody, BG694986 antibody, EST-c39 antibody, small integral membrane protein 19 antibody, SMIM19 antibody, Smim19 antibody
- 背景
-
Synonyms: C8orf40, CH040_HUMAN, UPF0697 protein C8orf40.
Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf40 gene product has been provisionally designated C8orf40 pending further characterization.
- 基因ID
- 114926
-
