Tricellulin 抗体 (AA 170-250)
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Quick Overview for Tricellulin 抗体 (AA 170-250) (ABIN7229556)
抗原
See all Tricellulin (MARVELD2) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 170-250
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原理
- Rabbit Anti-MALD2 Polyclonal Antibody
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特异性
- The antibody detects endogenous levels of MALD2 protein
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- Synthesized peptide derived from part region of human MALD2 protein at AA range: 170-250
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亚型
- IgG
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anti-Tricellulin (MARVELD2) (AA 200-300) antibody
MARVELD2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Tricellulin (MARVELD2) (AA 1-195) antibodyMARVELD2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Tricellulin (MARVELD2) (AA 251-300) antibodyMARVELD2 适用: 人, 小鼠, Cow, 犬, 马, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Tricellulin (MARVELD2) (AA 393-423), (C-Term) antibodyMARVELD2 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-Tricellulin (MARVELD2) (AA 386-415), (C-Term) antibodyMARVELD2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB24717 unconjugated
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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 1:500-2000,ELISA 1:5000-20000
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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, 50 % glycerol, 0.05 % Proclin 300, 0.05 %BSA
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储存液
- ProClin
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注意事项
- This product contains ProClin: 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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有效期
- 12 months
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- Tricellulin (MARVELD2)
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别名
- MALD2
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背景
- MARVEL domain-containing protein 2, TricellulinThe protein encoded by MARVELD2 (MARVEL Domain Containing 2) is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in MARVELD2 are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for MARVELD2.
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分子量
- 61kD
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基因ID
- 153562
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UniProt
- Q8N4S9
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途径
- Sensory Perception of Sound, Cell-Cell Junction Organization
抗原
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