CEACAM16 抗体 (AA 201-300)
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- 抗原 See all CEACAM16 抗体
- CEACAM16 (Carcinoembryonic Antigen-Related Cell Adhesion Molecule 16 (CEACAM16))
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抗原表位
- AA 201-300
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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 CEACAM16 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Cow,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CEACAM16
- 亚型
- IgG
- Top Product
- Discover our top product CEACAM16 Primary Antibody
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- CEACAM16 (Carcinoembryonic Antigen-Related Cell Adhesion Molecule 16 (CEACAM16))
- 别名
- CEACAM16 (CEACAM16 产品)
- 别名
- CEAL2 antibody, DFNA4B antibody, Gm769 antibody, Bcl3 antibody, carcinoembryonic antigen related cell adhesion molecule 16 antibody, carcinoembryonic antigen-related cell adhesion molecule 16 antibody, CEACAM16 antibody, Ceacam16 antibody
- 背景
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Synonyms: Carcinoembryonic antigen like 2, Carcinoembryonic antigen like 2 protein, Carcinoembryonic antigen related cell adhesion molecule 16, CEAL2, CEA16_HUMAN.
Background: The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause of non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012].
- 基因ID
- 388551
- 途径
- Sensory Perception of Sound
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