FSD2 抗体 (AA 221-320) (HRP)
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- 抗原 See all FSD2 抗体
- FSD2 (Fibronectin Type III and SPRY Domain Containing 2 (FSD2))
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抗原表位
- AA 221-320
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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 FSD2 antibody is conjugated to HRP
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FSD2
- 亚型
- IgG
- Top Product
- Discover our top product FSD2 Primary Antibody
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anti-Fibronectin Type III and SPRY Domain Containing 2 (FSD2) (N-Term) antibody
FSD2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Fibronectin Type III and SPRY Domain Containing 2 (FSD2) (AA 61-89), (N-Term) antibodyFSD2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB30189 unconjugated
anti-Fibronectin Type III and SPRY Domain Containing 2 (FSD2) (AA 61-89), (N-Term) antibodyFSD2 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 - 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
- FSD2 (Fibronectin Type III and SPRY Domain Containing 2 (FSD2))
- 别名
- FSD2 (FSD2 产品)
- 别名
- SPRYD1 antibody, 9830160G03Rik antibody, Spryd1 antibody, RGD1305167 antibody, fibronectin type III and SPRY domain containing 2 antibody, FSD2 antibody, Fsd2 antibody
- 背景
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Synonyms: Fibronectin type III and SPRY domain containing 2, Fibronectin type III and SPRY domain containing protein 2, RP11-127F21, SPRY domain containing 1, SPRY domain containing protein 1, SPRYD1,
Background: FSD2 is a 749 amino acid protein containing one B30.2/SPRY domain and two fibronectin type-III domains. The gene encoding FSD2 maps to human chromosome 15q25.2. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and consists of about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are also associated with chromosome 15.
- 基因ID
- 123722
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