TM9SF4 抗体 (AA 101-200) (AbBy Fluor® 350)
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- 抗原 See all TM9SF4 抗体
- TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))
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抗原表位
- AA 101-200
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适用
- 小鼠
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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 TM9SF4 antibody is conjugated to AbBy Fluor® 350
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human TM9SF4
- 亚型
- IgG
- Top Product
- Discover our top product TM9SF4 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
- TM9SF4 (Transmembrane 9 Superfamily Protein Member 4 (TM9SF4))
- 别名
- TM9SF4 (TM9SF4 产品)
- 别名
- dJ836N17.2 antibody, AA986553 antibody, AU045326 antibody, B930079E06 antibody, mKIAA0255 antibody, transmembrane 9 superfamily member 4 antibody, transmembrane 9 superfamily protein member 4 antibody, TM9SF4 antibody, Tm9sf4 antibody
- 背景
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Synonyms: dJ836N17.2, Transmembrane 9 superfamily member 4, TM9SF4, KIAA0255
Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis which are thought important for seminal production and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20.
- 基因ID
- 9777
- UniProt
- Q92544
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