Anti-FOXN1抗体(ab113235)
Key features and details
- Rabbit polyclonal to FOXN1
- Suitable for: WB, IHC-P
- Reacts with: Human
- Isotype: IgG
概述
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产品名称
Anti-FOXN1抗体
参阅全部 FOXN1 一抗 -
描述
兔多克隆抗体to FOXN1 -
宿主
Rabbit -
经测试应用
适用于: WB, IHC-Pmore details -
种属反应性
与反应: Human -
免疫原
Synthetic peptide, conjugated to KLH, corresponding to residues in Human FOXN1.
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阳性对照
- Human Uterus tissue; Raji whole cell lysate.
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常规说明
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
性能
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形式
Liquid -
存放说明
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles. -
存储溶液
pH: 7.00
Preservative: 0.01% Thimerosal (merthiolate)
Constituents: 10% Glycerol (glycerin, glycerine), 89% PBS -
Concentration information loading...
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纯度
Protein A purified -
克隆
多克隆 -
同种型
IgG -
研究领域
相关产品
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Compatible Secondaries
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Isotype control
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Positive Controls
应用
The Abpromise guarantee
Abpromise™承诺保证使用ab113235于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
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WB |
1/500 - 1/3000. Predicted molecular weight: 69 kDa.
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IHC-P |
Use a concentration of 10 µg/ml.
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说明 |
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WB
1/500 - 1/3000. Predicted molecular weight: 69 kDa. |
IHC-P
Use a concentration of 10 µg/ml. |
靶标
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功能
Transcriptional regulator involved in development. -
组织特异性
Expressed in thymus. -
疾病相关
Defects in FOXN1 are the cause of T-cell immunodeficiency congenital alopecia and nail dystrophy (TIDAND) [MIM:601705]. A disorder characterized by the association of congenital alopecia, severe T-cell immunodeficiency, and ridging and pitting of all nails. -
序列相似性
Contains 1 fork-head DNA-binding domain. -
细胞定位
Nucleus. - Information by UniProt
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数据库链接
- Entrez Gene: 8456 Human
- Omim: 600838 Human
- SwissProt: O15353 Human
- Unigene: 663679 Human
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别名
- FKHL20 antibody
- Forkhead box N1 antibody
- Forkhead box protein N1 antibody
see all
图片
数据表及文件
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SDS download
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Datasheet download
文献 (1)
ab113235 被引用在 1 文献中.
- Lin Z et al. Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia. Am J Hum Genet 91:906-11 (2012). PubMed: 23063621