CEA16 抗体
This 兔 多克隆 anti-CEA16 antibody specifically detects CEA16 in ELISA 和 WB. The antibody is reactive with 人 和 小鼠 samples.
产品编号 ABIN7227820
发货至:
中国
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中国
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北京 101111
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Quick Overview for CEA16 抗体 (ABIN7227820)
抗原
CEA16 (PSG28)
(Pregnancy-Specific Glycoprotein 28 (PSG28))
适用
人, 小鼠
宿主
兔
克隆类型
多克隆
标记
This CEA16 antibody is un-conjugated
应用范围
ELISA, Western Blotting (WB)
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原理
- CEA16 Polyclonal Antibody
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特异性
- The antibody detects endogenous levels of CEA16 protein
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纯化方法
- The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen
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免疫原
- Synthesized peptide derived from part region of human CEA16 protein
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亚型
- IgG
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), ELISA (1:5000-1:20000).
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说明
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Primary Antibody
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- CEA16 (PSG28) (Pregnancy-Specific Glycoprotein 28 (PSG28))
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别名
- CEA16
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背景
- Rabbit Anti-CEA16 Polyclonal Antibody,Carcinoembryonic antigen-related cell adhesion molecule 16, Carcinoembryonic antigen-like 2,CEACAM16 (Carcinoembryonic Antigen Related Cell Adhesion Molecule 16) is a Protein Coding gene. Diseases associated with CEACAM16 include Deafness, Autosomal Dominant 4B and Dfna 4B Nonsyndromic Hearing Loss And Deafness. 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 CEACAM16 likely are a cause of non-syndromic autosomal dominant hearing loss.,CEA16
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分子量
- observerd band 46kDa
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基因ID
- 388551
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UniProt
- Q2WEN9
抗原
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