BBS12 抗体 (AA 25-100) (FITC)
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- 抗原 See all BBS12 抗体
- BBS12 (Bardet-Biedl Syndrome 12 (BBS12))
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抗原表位
- AA 25-100
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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 BBS12 antibody is conjugated to FITC
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 预测反应
- Human,Mouse,Cow,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human BBS12
- 亚型
- IgG
- Top Product
- Discover our top product BBS12 Primary Antibody
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anti-Bardet-Biedl Syndrome 12 (BBS12) (AA 1-710) antibody
BBS12 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Bardet-Biedl Syndrome 12 (BBS12) antibodyBBS12 适用: 人 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
- BBS12 (Bardet-Biedl Syndrome 12 (BBS12))
- 别名
- BBS12 (BBS12 产品)
- 别名
- Gm1805 antibody, Gm407 antibody, Gm721 antibody, RP23-137F6.2 antibody, RGD1561608 antibody, C4orf24 antibody, DKFZP468P0511 antibody, Bardet-Biedl syndrome 12 (human) antibody, Bardet-Biedl syndrome 12 antibody, Bardet-Biedl syndrome 12 L homeolog antibody, Bbs12 antibody, BBS12 antibody, bbs12 antibody, bbs12.L antibody
- 背景
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Synonyms: Bardet Biedl syndrome 12 protein, Bardet-Biedl syndrome 12 human, Bardet-Biedl syndrome 12 protein homolog, BBS12 gene, C4orf24, FLJ35630, FLJ41559, Gm1805, Gm407, Gm721, RP23-137F6.2,BBS12_HUMAN.
Background: The protein encoded by this gene is part of a complex that is involved in membrane trafficking. The encoded protein is a molecular chaperone that aids in protein folding upon ATP hydrolysis. This protein also plays a role in adipocyte differentiation. Defects in this gene are a cause of Bardet-Biedl syndrome type 12. Two transcript variants encoding the same protein have been found for this gene.
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