FAM221A 抗体 (AA 201-298)
FAM221A
适用: 人
WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p), ICC
宿主: 兔
Polyclonal
unconjugated
-
- 抗原 See all FAM221A 抗体
- FAM221A (Family with Sequence Similarity 221, Member A (FAM221A))
- 抗原表位
- AA 201-298
- 适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This FAM221A antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7orf46
- 亚型
- IgG
-
-
- 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
- FAM221A (Family with Sequence Similarity 221, Member A (FAM221A))
- 别名
- C7orf46 (FAM221A 产品)
- 别名
- C7orf46 antibody, D330028D13Rik antibody, c7orf46 antibody, family with sequence similarity 221 member A antibody, family with sequence similarity 221, member A antibody, family with sequence similarity 221 member A L homeolog antibody, FAM221A antibody, Fam221a antibody, fam221a.L antibody
- 背景
-
Synonyms: C7orf46, F221A_HUMAN, Chromosome 7 open reading frame 46, Uncharacterized protein C7orf46.
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 C7orf46 gene product has been provisionally designated C7orf46 pending further characterization.
-
You are here:
