LSMEM1 抗体 (AA 31-100)
-
- 抗原 See all LSMEM1 (C7ORF53) 抗体
- LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
-
抗原表位
- AA 31-100
- 适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This LSMEM1 antibody is un-conjugated
-
应用范围
- ELISA, Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunocytochemistry (ICC)
- 预测反应
- Human,Mouse,Rat,Dog
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7orf53
- 亚型
- IgG
- Top Product
- Discover our top product C7ORF53 Primary Antibody
-
anti-Chromosome 7 Open Reading Frame 53 (C7ORF53) (AA 1-131) antibody
C7ORF53 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
-
WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
-
- 抗原
- LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
- 别名
- C7orf53 (C7ORF53 产品)
- 别名
- C7orf53 antibody, Gm889 antibody, C4H7orf53 antibody, C1H7orf53 antibody, C7ORF53 antibody, leucine rich single-pass membrane protein 1 antibody, leucine-rich single-pass membrane protein 1 antibody, LSMEM1 antibody, Lsmem1 antibody
- 背景
-
Synonyms: C7orf53, CG053_HUMAN, Chromosome 7 open reading frame 53, Coiled-coil domain-containing transmembrane protein C7orf53.
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 C7orf53 gene product has been provisionally designated C7orf53 pending further characterization.
- 基因ID
- 286006
-
