BSPRY 抗体 (AA 251-350) (FITC)
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- 抗原 See all BSPRY 抗体
- BSPRY (B-Box and SPRY Domain Containing (BSPRY))
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抗原表位
- AA 251-350
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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 BSPRY antibody is conjugated to FITC
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human BSPRY
- 亚型
- IgG
- Top Product
- Discover our top product BSPRY Primary Antibody
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anti-B-Box and SPRY Domain Containing (BSPRY) (AA 1-193) antibody
BSPRY 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-B-Box and SPRY Domain Containing (BSPRY) (AA 118-167) antibodyBSPRY 适用: 人, Cow, 大鼠, 犬, 马, 小鼠, 猴 WB 宿主: 兔 Polyclonal unconjugated
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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
- BSPRY (B-Box and SPRY Domain Containing (BSPRY))
- 别名
- BSPRY (BSPRY 产品)
- 别名
- B-box and SPRY domain containing antibody, BSPRY antibody, Bspry antibody
- 背景
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Synonyms: B box and SPRY domain containing, B box and SPRY domain containing protein, B box and SPRY domain-containing protein,B-box and SPRY domain containing, Bspry, BSPRY_HUMAN, FLJ20150, Zetin 1.
Background: BSPRY is a 402 amino acid protein that localizes to both the membrane and the cytoplasm and contains one B box-type zinc finger and one B30.2/SPRY domain. Existing as two alternatively spliced isoforms, BSPRY interacts with TRPV5 and TRPV6 and is thought to regulate the transport of calcium across the epithelium, probably by inhibiting the activity of TRPV proteins. The gene encoding BSPRY maps to human chromosome 9, which houses over 900 genes and comprises nearly 4 % of the human genome. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and Familial dysautonomia, are both associated with chromosome 9. Notably, chromosome 9 encompasses the largest interferon family gene cluster.
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