FAM160B1 抗体 (AA 521-630)
Quick Overview for FAM160B1 抗体 (AA 521-630) (ABIN873209)
抗原
See all FAM160B1 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 521-630
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预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Chicken,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 FAM160B1
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亚型
- IgG
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anti-Family with Sequence Similarity 160, Member B1 (FAM160B1) (AA 35-84) antibody
FAM160B1 适用: 人, 小鼠, Cow, 犬, 豚鼠, 马, 兔, 大鼠, 斑马鱼, Bat, 小鸡, 猴, Pig, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 160, Member B1 (FAM160B1) (N-Term) antibodyFAM160B1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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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储存条件
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- FAM160B1 (Family with Sequence Similarity 160, Member B1 (FAM160B1))
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别名
- Fam160b1
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背景
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Synonyms: DKFZp686D10123, F16B1_HUMAN, Fam160b1, Family with sequence similarity 160 member B1, Hypothetical protein LOC57700, KIAA1600, Protein FAM160B1.
Background: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.
抗原
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