MSANTD3 抗体 (AA 1-100) (HRP)
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北京 101111
Quick Overview for MSANTD3 抗体 (AA 1-100) (HRP) (ABIN1712122)
抗原
See all MSANTD3 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 1-100
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交叉反应
- 人
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预测反应
- Mouse,Rat,Dog,Sheep,Pig,Horse,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human C9orf30
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亚型
- IgG
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anti-Myb/SANT-Like DNA-Binding Domain Containing 3 (MSANTD3) (AA 1-100) antibody
MSANTD3 适用: 人 WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
anti-Myb/SANT-Like DNA-Binding Domain Containing 3 (MSANTD3) (AA 1-275) antibodyMSANTD3 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- MSANTD3 (Myb/SANT-Like DNA-Binding Domain Containing 3 (MSANTD3))
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别名
- C9orf30
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背景
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Synonyms: Chromosome 9 open reading frame 30, CI030, FLJ34973, Hypothetical protein LOC91283, L8, MGC17337, OTTHUMP00000021792, UPF0439 protein C9orf30, MSD3_HUMAN.
Background: C9orf30 is a 275 amino acid protein that is expressed in brain and belongs to the UPF0439 family. The gene encoding C9orf30 maps to human chromosome 9q31.1. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
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基因ID
- 91283
抗原
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