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- 抗原 See all Claudin 19 (CLDN19) 抗体
- Claudin 19 (CLDN19)
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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 Claudin 19 antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (IHC)
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Antigen affinity purification
- 免疫原
- Synthetic peptide of Human CLDN19
- 亚型
- IgG
- Top Product
- Discover our top product CLDN19 Primary Antibody
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anti-Claudin 19 (CLDN19) (AA 1-211) antibody
CLDN19 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2F2 unconjugated
anti-Claudin 19 (CLDN19) (AA 21-120) antibodyCLDN19 适用: 小鼠 ELISA, IF (p), IF (cc), IHC (fro), IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
anti-Claudin 19 (CLDN19) (Internal Region) antibodyCLDN19 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Claudin 19 (CLDN19) (AA 1-211) antibodyCLDN19 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Claudin 19 (CLDN19) (Internal Region) antibodyCLDN19 适用: 人, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Claudin 19 (CLDN19) (Internal Region) antibodyCLDN19 适用: 人, 大鼠 WB, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Claudin 19 (CLDN19) (C-Term) antibodyCLDN19 适用: 人, 小鼠, Cow, Pig, 兔, 犬, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Claudin 19 (CLDN19) (C-Term) antibodyCLDN19 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- ELISA:1:2000-1:5000, IHC:1:25-1:100,
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- 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,-80 °C
- 储存方法
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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- 抗原
- Claudin 19 (CLDN19)
- 别名
- CLDN19 (CLDN19 产品)
- 别名
- HOMG5 antibody, claudin-19 antibody, zgc:112141 antibody, claudin 19 antibody, claudin 19 S homeolog antibody, CLDN19 antibody, Cldn19 antibody, cldn19.S antibody, cldn19 antibody
- 背景
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Background: The product of this gene belongs to the claudin family. It plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. Defects in this gene are the cause of hypomagnesemia renal with ocular involvement (HOMGO). HOMGO is a progressive renal disease characterized by primary renal magnesium wasting with hypomagnesemia, hypercalciuria and nephrocalcinosis associated with severe ocular abnormalities such as bilateral chorioretinal scars, macular colobomata, significant myopia and nystagmus. Alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene.
Aliases: CLDN19Claudin-19 antibody
- UniProt
- Q8N6F1
- 途径
- Cell-Cell Junction Organization, Hepatitis C
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