FUNDC2 抗体
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北京 101111
Quick Overview for FUNDC2 抗体 (ABIN7246850)
抗原
See all FUNDC2 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Antigen affinity purification
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免疫原
- Fusion protein of human FUNDC2
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亚型
- IgG
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anti-FUN14 Domain Containing 2 (FUNDC2) (AA 122-150), (C-Term) antibody
FUNDC2 适用: 小鼠 WB 宿主: 兔 Polyclonal RB40833 unconjugated
anti-FUN14 Domain Containing 2 (FUNDC2) (AA 1-100) antibodyFUNDC2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 2G12 unconjugated
anti-FUN14 Domain Containing 2 (FUNDC2) (AA 1-189) antibodyFUNDC2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-FUN14 Domain Containing 2 (FUNDC2) (AA 1-189) antibodyFUNDC2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-FUN14 Domain Containing 2 (FUNDC2) (AA 1-100) antibodyFUNDC2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4D7 unconjugated
anti-FUN14 Domain Containing 2 (FUNDC2) (AA 24-73) antibodyFUNDC2 适用: 人, 猴 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-FUN14 Domain Containing 2 (FUNDC2) (N-Term) antibodyFUNDC2 适用: 人, Cow, 犬, 马, Pig, 兔 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC 1:50-1:300, ELISA 1:5000-1:10000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.72 mg/mL
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缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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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
- Store at -20°C. Avoid freeze / thaw cycles.
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- FUNDC2 (FUN14 Domain Containing 2 (FUNDC2))
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别名
- FUNDC2
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背景
- FUNDC2 (FUN14 domain-containing protein 2), also known as HCC-3 (cervical cancer proto-oncogene 3 protein), HCBP6 (hepatitis C virus core-binding protein 6) or DC44, is a 189 amino acid protein belonging to the FUN14 family. The gene encoding FUNDC2 maps to human chromosome Xq28. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
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UniProt
- Q9BWH2
抗原
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