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- 抗原 See all CLDND1 抗体
- CLDND1 (Claudin Domain Containing 1 (CLDND1))
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适用
- 人, 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 CLDND1 antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (IHC)
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human CLDND1
- 亚型
- IgG
- Top Product
- Discover our top product CLDND1 Primary Antibody
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anti-Claudin Domain Containing 1 (CLDND1) antibody
CLDND1 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Claudin Domain Containing 1 (CLDND1) (AA 26-140) antibodyCLDND1 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Claudin Domain Containing 1 (CLDND1) (AA 110-159) antibodyCLDND1 适用: 人, 小鼠, 大鼠, Pig, 兔, 犬, 马, 猴 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IHC 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.2 mg/mL
- 缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- CLDND1 (Claudin Domain Containing 1 (CLDND1))
- 别名
- CLDND1 (CLDND1 产品)
- 别名
- MGC53751 antibody, LOC100217896 antibody, 1110019C08Rik antibody, AA407103 antibody, AI849195 antibody, AW489850 antibody, Cldnd1 antibody, C3orf4 antibody, GENX-3745 antibody, claudin domain containing 1 L homeolog antibody, claudin domain containing 1 antibody, cldnd1.L antibody, cldnd1 antibody, CLDND1 antibody, Cldnd1 antibody
- 背景
- CLDND1 (claudin domain containing 1), also known as C3orf4 or HSPC174, is a 253 amino acid multi-pass membrane protein that is expressed at high levels in adult brain and at lower levels in adult heart. Existing as two alternatively spliced isoforms, CLDND1 is encoded by a gene that maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
- UniProt
- Q9NY35
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