FAM160B1 抗体 (AA 521-630) (Alexa Fluor 750)
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- 抗原 See all FAM160B1 抗体
- FAM160B1 (Family with Sequence Similarity 160, Member B1 (FAM160B1))
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抗原表位
- AA 521-630
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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 FAM160B1 antibody is conjugated to Alexa Fluor 750
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM160B1
- 亚型
- IgG
- Top Product
- Discover our top product FAM160B1 Primary Antibody
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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
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- 应用备注
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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
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- FAM160B1 (Family with Sequence Similarity 160, Member B1 (FAM160B1))
- 别名
- FAM160B1 (FAM160B1 产品)
- 别名
- zgc:162264 antibody, kiaa1600 antibody, KIAA1600 antibody, bA106M7.3 antibody, AI450540 antibody, mKIAA1600 antibody, RGD1306116 antibody, family with sequence similarity 160, member B1 antibody, family with sequence similarity 160 member B1 antibody, family with sequence similarity 160 member B1 S homeolog antibody, fam160b1 antibody, FAM160B1 antibody, Fam160b1 antibody, fam160b1.S antibody
- 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.
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