KIAA1522 抗体 (AA 101-250)
-
- 抗原 See all KIAA1522 products
- KIAA1522
-
抗原表位
- AA 101-250
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This KIAA1522 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), ELISA, Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human KIAA1522
- 亚型
- IgG
-
-
- 应用备注
-
WB 1:300-5000
ELISA 1:500-1000
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 限制
- 仅限研究用
-
- 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
-
-
KIAA1522 is a novel prognostic biomarker in patients with non-small cell lung cancer." in: Scientific reports, Vol. 6, pp. 24786, (2017) (PubMed).
: "
-
KIAA1522 is a novel prognostic biomarker in patients with non-small cell lung cancer." in: Scientific reports, Vol. 6, pp. 24786, (2017) (PubMed).
-
- 抗原
- KIAA1522
- 别名
- KIAA1522 (KIAA1522 产品)
- 别名
- Kiaa1522 antibody, mKIAA1522 antibody, expressed sequence C77080 antibody, KIAA1522 antibody, KIAA1522 ortholog antibody, C77080 antibody, KIAA1522 antibody
- 背景
-
Synonyms: K1522_HUMAN, Kiaa1522, Uncharacterized protein KIAA1522.
Background: KIAA1522 is a 1,035 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 1p35.1. Chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.
- 基因ID
- 57648
-