Tricellulin 抗体
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- 抗原 See all Tricellulin (MARVELD2) 抗体
- Tricellulin (MARVELD2)
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适用
- 人, 大鼠, 小鼠
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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 Tricellulin antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- 纯化方法
- Immunogen affinity purified
- 纯度
- ≥95 % as determined by SDS-PAGE
- 免疫原
- MARVEL domain containing 2
- 亚型
- IgG
- Top Product
- Discover our top product MARVELD2 Primary Antibody
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anti-Tricellulin (MARVELD2) antibody
MARVELD2 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Tricellulin (MARVELD2) (AA 251-300) antibodyMARVELD2 适用: 人, 小鼠, Cow, 犬, 马, 猴, Bat WB 宿主: 兔 Polyclonal unconjugated
anti-Tricellulin (MARVELD2) (AA 200-300) antibodyMARVELD2 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 386-415), (C-Term) antibodyMARVELD2 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB24717 unconjugated
anti-Tricellulin (MARVELD2) (AA 393-423), (C-Term) antibodyMARVELD2 适用: 人 WB, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
- 有效期
- 12 months
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- 抗原
- Tricellulin (MARVELD2)
- 别名
- MARVELD2 (MARVELD2 产品)
- 别名
- Mrvldc2 antibody, BC003296 antibody, MARVD2 antibody, Tric antibody, Trica antibody, Tricb antibody, Tricc antibody, DFNB49 antibody, MRVLDC2 antibody, MARVEL domain containing 2 antibody, MARVEL (membrane-associating) domain containing 2 antibody, Marveld2 antibody, MARVELD2 antibody
- 背景
- Synonyms:TRIC Background:The protein encoded by this gene 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 this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.
- 分子量
- 69 kDa
- 基因ID
- 153562
- UniProt
- Q8N4S9
- 途径
- Sensory Perception of Sound, Cell-Cell Junction Organization
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