CCDC115 抗体 (AA 1-180) (PE)
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北京 101111
Quick Overview for CCDC115 抗体 (AA 1-180) (PE) (ABIN7980904)
抗原
See all CCDC115 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 1-180
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原理
- Anti-CCDC115 Antibody PE Conjugated
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交叉反应 （详细）
- No cross-reactivity with other proteins
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human CCDC115 recombinant protein (Position: M1-A180).
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亚型
- IgG
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anti-Coiled-Coil Domain Containing 115 (CCDC115) (AA 1-132) antibody
CCDC115 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 4E9 unconjugated
anti-Coiled-Coil Domain Containing 115 (CCDC115) (AA 1-180) antibodyCCDC115 适用: 人 WB, ELISA, FACS, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 115 (CCDC115) (AA 1-180) antibodyCCDC115 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 115 (CCDC115) (AA 47-96) antibodyCCDC115 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 115 (CCDC115) (N-Term) antibodyCCDC115 适用: 人, Cow, 犬, Pig WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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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
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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- CCDC115 (Coiled-Coil Domain Containing 115 (CCDC115))
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别名
- CCDC115
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背景
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Background: Coiled-coil domain containing 115 is a protein that in humans is encoded by the CCDC115 gene. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) vesicles in some human cells. The encoded protein shares some homology with the yeast V-ATPase assembly factor Vma22p, and the orthologous protein in mouse promotes cell proliferation and suppresses cell death. Defects in this gene are a cause of congenital disorder of glycosylation, type IIo in humans.
Gene Full Name: vacuolar ATPase assembly factor VMA22
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基因ID
- 84317
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UniProt
- Q96NT0
抗原
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