FAM92A1 抗体 (AA 101-200)
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- 抗原 See all FAM92A1 抗体
- FAM92A1 (Family with Sequence Similarity 92, Member A1 (FAM92A1))
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抗原表位
- AA 101-200
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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 FAM92A1 antibody is un-conjugated
- 应用范围
- ELISA, Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunocytochemistry (ICC)
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM92A1
- 亚型
- IgG
- Top Product
- Discover our top product FAM92A1 Primary Antibody
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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
ICC 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
- 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
- FAM92A1 (Family with Sequence Similarity 92, Member A1 (FAM92A1))
- 别名
- FAM92A1 (FAM92A1 产品)
- 别名
- RGD1310681 antibody, fam92a1-b antibody, zgc:100998 antibody, 6720467C03Rik antibody, Fam92a1 antibody, family with sequence similarity 92 member A antibody, ffamily with sequence similarity 92 member A L homeolog antibody, family with sequence similarity 92, member A1 antibody, protein FAM92A antibody, family with sequence similarity 92, member A antibody, family with sequence similarity 92 member A S homeolog antibody, FAM92A antibody, Fam92a antibody, fam921.L antibody, fam92a1 antibody, fam921.S antibody
- 背景
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Synonyms: Family with sequence similarity 92, member A1, FLJ38979, Hypothetical protein LOC137392, Protein FAM92A1, F92A1_HUMAN.
Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM92A1 gene product has been provisionally designated FAM92A1 pending further characterization.
- 基因ID
- 137392
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