FHAD1 抗体 (AA 401-500) (Biotin)
-
- 抗原 See all FHAD1 products
- FHAD1 (Forkhead-Associated (FHA) Phosphopeptide Binding Domain 1 (FHAD1))
-
抗原表位
- AA 401-500
- 适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This FHAD1 antibody is conjugated to Biotin
-
应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 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
-
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
-
- 应用备注
-
IHC-P 1:200-400
IHC-F 1:100-500 - 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 for 12 months.
- 有效期
- 12 months
-
- 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
-
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
-
