MSANTD3 抗体 (AA 1-100) (Biotin)
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- 抗原 See all MSANTD3 抗体
- MSANTD3 (Myb/SANT-Like DNA-Binding Domain Containing 3 (MSANTD3))
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抗原表位
- AA 1-100
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适用
- 人
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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 MSANTD3 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C9orf30
- 亚型
- IgG
- Top Product
- Discover our top product MSANTD3 Primary Antibody
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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), IHC (fro), IHC (p), ELISA, 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
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- MSANTD3 (Myb/SANT-Like DNA-Binding Domain Containing 3 (MSANTD3))
- 别名
- C9orf30 (MSANTD3 产品)
- 别名
- C9orf30 antibody, C8H9orf30 antibody, 2410046L14Rik antibody, 2810429P03Rik antibody, 5730528L13Rik antibody, Mysantd3 antibody, c9orf30 antibody, Myb/SANT DNA binding domain containing 3 antibody, Myb/SANT-like DNA-binding domain containing 3 antibody, Myb/SANT DNA binding domain containing 3 L homeolog antibody, MSANTD3 antibody, Msantd3 antibody, msantd3.L antibody
- 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.
- 基因ID
- 91283
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