FOXN1 抗体 (AA 321-420) (AbBy Fluor® 488)
-
- 抗原 See all FOXN1 抗体
- FOXN1 (Forkhead Box N1 (FOXN1))
-
抗原表位
- AA 321-420
-
适用
- 人, 大鼠, 小鼠
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This FOXN1 antibody is conjugated to AbBy Fluor® 488
-
应用范围
- Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 预测反应
- Dog,Cow,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FOXN1
- 亚型
- IgG
- Top Product
- Discover our top product FOXN1 Primary Antibody
-
-
- 应用备注
-
FCM 1:20-100
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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
- FOXN1 (Forkhead Box N1 (FOXN1))
- 别名
- FOXN1 (FOXN1 产品)
- 别名
- nude antibody, whnb antibody, FOXN1 antibody, foxN1 antibody, foxN antibody, foxn1 antibody, FKHL20 antibody, RONU antibody, WHN antibody, D11Bhm185e antibody, Fkh19 antibody, HFH-11 antibody, Hfh11 antibody, Whn antibody, nu antibody, Rnu antibody, forkhead box N1 antibody, forkhead box protein N1 antibody, FOXN1 antibody, foxn1 antibody, foxN1 antibody, LOC100125524 antibody, Foxn1 antibody
- 背景
-
Synonyms: WHN, RONU, FKHL20, Forkhead box protein N1, Winged-helix transcription factor nude, FOXN1
Background: Mutations in the winged-helix transcription factor gene at the nude locus in mice and rats produce the pleiotropic phenotype of hairlessness and athymia, resulting in a severely compromised immune system. This gene is orthologous to the mouse and rat genes and encodes a similar DNA-binding transcription factor that is thought to regulate keratin gene expression. A mutation in this gene has been correlated with T-cell immunodeficiency, the skin disorder congenital alopecia, and nail dystrophy. Alternative splicing in the 5' UTR of this gene has been observed. [provided by RefSeq, Jul 2008].
- 基因ID
- 8456
- UniProt
- O15353
-