FAM55A 抗体 (AA 211-310) (Alexa Fluor 555)
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- 抗原 See all FAM55A products
- FAM55A (Family with Sequence Similarity 55, Member A (FAM55A))
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抗原表位
- AA 211-310
- 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 FAM55A antibody is conjugated to Alexa Fluor 555
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human FAM55A
- 亚型
- IgG
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anti-Family with Sequence Similarity 55, Member A (FAM55A) (AA 1-405) antibody
FAM55A 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Family with Sequence Similarity 55, Member A (FAM55A) (AA 1-405) antibodyFAM55A 适用: 人 WB 宿主: 小鼠 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
- FAM55A (Family with Sequence Similarity 55, Member A (FAM55A))
- 别名
- FAM55A (FAM55A 产品)
- 别名
- FAM55A antibody, neurexophilin and PC-esterase domain family member 1 antibody, neurexophilin and PC-esterase domain family, member 1 antibody, NXPE1 antibody
- 背景
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Synonyms: FA55A_HUMAN, FAM55A, Family with sequence similarity 55, member A, Hypothetical protein LOC120400, MGC34290, Neurexophilin and PC-esterase domain family, member 1, NXPE family member 1, NXPE1, OTTHUMP00000238511, Protein FAM55A.
Background: With approximately 135 million base pairs and 1,400 genes, chromosome 11 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. The FAM55A gene product has been provisionally designated FAM55A pending further characterization.
- 基因ID
- 120400
- UniProt
- Q8N323
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