RNF215 抗体 (AbBy Fluor® 350)
-
- 抗原 See all RNF215 抗体
- RNF215 (Ring Finger Protein 215 (RNF215))
- 适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This RNF215 antibody is conjugated to AbBy Fluor® 350
-
应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human RNF215
- 亚型
- IgG
- Top Product
- Discover our top product RNF215 Primary Antibody
-
anti-Ring Finger Protein 215 (RNF215) (AA 266-295), (C-Term) antibody
RNF215 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB29703 unconjugated
anti-Ring Finger Protein 215 (RNF215) (AA 273-303), (C-Term) antibodyRNF215 适用: 人, 小鼠 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
-
- 应用备注
- IF(IHC-P) 1:50-200
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
-
- 抗原
- RNF215 (Ring Finger Protein 215 (RNF215))
- 别名
- RNF215 (RNF215 产品)
- 别名
- RGD1310738 antibody, 0610009J22Rik antibody, AW557025 antibody, C77903 antibody, ring finger protein 215 antibody, Rnf215 antibody, RNF215 antibody
- 背景
-
Synonyms: RING finger protein 215, Rnf215, RN215_HUMAN.
Background: The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF215 (ring finger protein 215), is a 377 amino acid multi-pass membrane protein containing one RING-type zinc finger. The gene encoding RNF215 maps to human chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, Neurofibromatosis type 2, autism and schizophrenia.
- 基因ID
- 200312
- UniProt
- Q9Y6U7
-
