FOXN1 抗体 (AA 321-420)
(1 reference)Quick Overview for FOXN1 抗体 (AA 321-420) (ABIN1387592)
抗原
See all FOXN1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 321-420
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交叉反应
- 人, 小鼠, 大鼠
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预测反应
- Dog,Cow,Pig,Horse,Chicken,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human FOXN1
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亚型
- IgG
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anti-Forkhead Box N1 (FOXN1) (AA 1-160) antibody
FOXN1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box N1 (FOXN1) (C-Term) antibodyVerified FOXN1 适用: 人 ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Forkhead Box N1 (FOXN1) (C-Term) antibodyFOXN1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box N1 (FOXN1) (N-Term) antibodyFOXN1 适用: 人, 大鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box N1 (FOXN1) (AA 51-100) antibodyFOXN1 适用: 人, 大鼠, 小鼠, 犬, 豚鼠, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Forkhead Box N1 (FOXN1) (AA 350-378) antibodyFOXN1 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB32003 unconjugated
anti-Forkhead Box N1 (FOXN1) (AA 357-386), (Middle Region) antibodyFOXN1 适用: 人 WB, FACS, EIA 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
ELISA 1:500-1000
FCM 1:20-100
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 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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: "EXTL3
mutations cause skeletal dysplasia, immune deficiency, and developmental delay. ..." in: The Journal of experimental medicine, Vol. 214, Issue 3, pp. 623-637, (2017) (PubMed).
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: "EXTL3
mutations cause skeletal dysplasia, immune deficiency, and developmental delay. ..." in: The Journal of experimental medicine, Vol. 214, Issue 3, pp. 623-637, (2017) (PubMed).
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- FOXN1 (Forkhead Box N1 (FOXN1))
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别名
- FOXN1
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背景
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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].
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基因ID
- 8456
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UniProt
- O15353
抗原
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