FGFBP2 抗体 (AA 121-220) (AbBy Fluor® 647)
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- 抗原 See all FGFBP2 抗体
- FGFBP2 (Fibroblast Growth Factor Binding Protein 2 (FGFBP2))
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抗原表位
- AA 121-220
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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 FGFBP2 antibody is conjugated to AbBy Fluor® 647
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FGFBP2/KSP37
- 亚型
- IgG
- Top Product
- Discover our top product FGFBP2 Primary Antibody
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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
- FGFBP2 (Fibroblast Growth Factor Binding Protein 2 (FGFBP2))
- 别名
- FGFBP2/KSP37 (FGFBP2 产品)
- 别名
- fb08g06 antibody, wu:fb08g06 antibody, HBP17RP antibody, KSP37 antibody, fibroblast growth factor binding protein 2 antibody, fibroblast growth factor binding protein 2a antibody, fibroblast growth factor binding protein 2 L homeolog antibody, FGFBP2 antibody, fgfbp2a antibody, fgfbp2.L antibody
- 背景
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Synonyms: FGF-binding protein 2, FGF-BP2, FGFBP-2, FGFBP2, FGFP2_HUMAN, Fibroblast growth factor-binding protein 2, HBp17-related protein, HBp17-RP, Ksp37, 37 kDa killer-specic secretory protein.
Background: KSP37 is a 223 amino acid protein that is secreted into the extracellular space and belongs to the fibroblast growth factor-binding protein family. Expressed in serum, as well as in cytotoxic T lymphocytes and peripheral leukocytes, KSP37 is thought to be involved in lymphocyte-mediated immunity, possibly playing a role in the development of asthma. The gene encoding KSP37 maps to human chromosome 4, which encodes nearly 6 % of the human genome and has the largest gene deserts (regions of the genome with no protein encoding genes) of all of the human chromosomes. Defects in some of the genes located on chromosome 4 are associated with Huntington's disease, Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease.
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