MB21D2 抗体
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- 抗原 See all MB21D2 products
- MB21D2 (Mab-21 Domain Containing 2 (MB21D2))
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适用
- 人, 小鼠, 大鼠
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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 MB21D2 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C3orf59/MB21D2
- 亚型
- IgG
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anti-Mab-21 Domain Containing 2 (MB21D2) (C-Term) antibody
MB21D2 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼, 小鸡, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Mab-21 Domain Containing 2 (MB21D2) (C-Term) antibodyMB21D2 适用: 人, 小鼠, 大鼠, Cow, 犬, 豚鼠, 马, 兔, 斑马鱼 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- MB21D2 (Mab-21 Domain Containing 2 (MB21D2))
- 别名
- C3orf59 (MB21D2 产品)
- 别名
- C3orf59 antibody, 1600021P15Rik antibody, A430031N04 antibody, C87006 antibody, Mab-21 domain containing 2 antibody, chromosome 3 open reading frame 59 antibody, MB21D2 antibody, c3orf59 antibody, Mb21d2 antibody
- 背景
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Synonyms: Protein MB21D2, Mab-21 domain-containing protein 2, M21D2_HUMAN.
Background: Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and 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. The C3orf59 gene product has been provisionally designated C3orf59 pending further characterization.
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