FHAD1 抗体 (AA 401-500) (Cy5)
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- 抗原 See all FHAD1 products
- FHAD1 (Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1))
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抗原表位
- AA 401-500
- 适用
- 人
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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 FHAD1 antibody is conjugated to Cy5
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应用范围
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 预测反应
- Human,Mouse,Rat,Cow,Sheep,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FHAD1
- 亚型
- IgG
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anti-Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1) (AA 1145-1173), (C-Term) antibody
FHAD1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB29504 unconjugated
anti-Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1) (AA 1152-1181), (C-Term) antibodyFHAD1 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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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
- 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
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- 抗原
- FHAD1 (Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1))
- 别名
- FHAD1 (FHAD1 产品)
- 别名
- 2900090M10Rik antibody, B230311F11 antibody, RGD1563444 antibody, forkhead associated phosphopeptide binding domain 1 antibody, forkhead-associated (FHA) phosphopeptide binding domain 1 antibody, FHAD1 antibody, Fhad1 antibody
- 背景
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Synonyms: FHA domain-containing protein 1, Forkhead-associated FHA phosphopeptide binding domain, Forkhead-associated domain-containing protein 1, KIAA1937, RP3-467K16.1, FHAD1_HUMAN.
Background: The FHAD1 gene encodes a 1,420 amino acid protein and maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
- 基因ID
- 114827
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