ZSWIM3 抗体 (Alexa Fluor 488)
-
- 抗原 See all ZSWIM3 products
- ZSWIM3 (Zinc Finger, SWIM-Type Containing 3 (ZSWIM3))
-
适用
- 人, 小鼠, 大鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This ZSWIM3 antibody is conjugated to Alexa Fluor 488
-
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 ZSWIM3
- 亚型
- IgG
-
anti-Zinc Finger, SWIM-Type Containing 3 (ZSWIM3) (AA 35-84) antibody
ZSWIM3 适用: 人, 小鼠, 大鼠, 马, Pig, Bat WB 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
- ZSWIM3 (Zinc Finger, SWIM-Type Containing 3 (ZSWIM3))
- 别名
- ZSWIM3 (ZSWIM3 产品)
- 别名
- 4921517A06Rik antibody, C86566 antibody, C20orf164 antibody, zinc finger SWIM-type containing 3 antibody, zinc finger, SWIM-type containing 3 antibody, ZSWIM3 antibody, Zswim3 antibody
- 背景
-
Synonyms: Zinc finger SWIM domain containing protein 3, C20orf164, Zinc finger SWIM type containing 3, ZSWIM 3, ZSWM3_HUMAN.
Background: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. ZSWIM3 (Zinc finger SWIM domain-containing protein 3) is a 696 amino acid protein that contains one SWIM-type zinc finger. SWIM domains are found in a variety of eukaryotic and prokaryotic proteins and are thought to be critical for certain ubiquitination reactions. The gene encoding ZSWIM3 maps to human chromosome 20, which contains nearly 63 million bases that encode over 600 genes, some of which are associated with Creutzfeldt-Jakob disease, amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome.
- 基因ID
- 140831
-
