FCHSD1 抗体 (AA 151-250)
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- 抗原 See all FCHSD1 products
- FCHSD1 (Similar To FCH and Double SH3 Domains 1 (FCHSD1))
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抗原表位
- AA 151-250
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适用
- 人, 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This FCHSD1 antibody is un-conjugated
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应用范围
- ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人, 小鼠
- 预测反应
- Rat,Dog,Cow,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FCHSD1
- 亚型
- IgG
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anti-Similar To FCH and Double SH3 Domains 1 (FCHSD1) (AA 100-400) antibody
FCHSD1 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Similar To FCH and Double SH3 Domains 1 (FCHSD1) (AA 1-409) antibodyFCHSD1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Similar To FCH and Double SH3 Domains 1 (FCHSD1) (C-Term) antibodyFCHSD1 适用: 人, 小鼠 WB, ELISA, IHC (p), IHC 宿主: 小鸡 Polyclonal unconjugated
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- 应用备注
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ELISA 1:500-1000
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
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- FCHSD1 (Similar To FCH and Double SH3 Domains 1 (FCHSD1))
- 别名
- FCHSD1 (FCHSD1 产品)
- 别名
- NWK2 antibody, A030002D08Rik antibody, FCH and double SH3 domains 1 antibody, Fchsd1 antibody, FCHSD1 antibody
- 背景
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Synonyms: FCH and double SH3 domains 1, FCH and double SH3 domains protein 1, FCHSD 1, FCHSD1, FCSD1_HUMAN, FLJ00007, Nervous wreck homolog 2, NWK 2, NWK2.
Background: FCHSD1 is a 690 amino acid protein that contains one FCH domain and two SH3 domains. FCHSD1 exists as three isoforms as a result of alternative splicing events. The gene encoding FCHSD1 maps to chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
- 基因ID
- 89848
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