ESYT1 抗体 (AA 651-750)
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- 抗原 See all ESYT1 抗体
- ESYT1 (Extended Synaptotagmin-Like Protein 1 (ESYT1))
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抗原表位
- AA 651-750
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适用
- 人, 小鼠
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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 ESYT1 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人, 小鼠
- 预测反应
- Rat,Dog,Cow,Pig,Horse,Rabbit,Monkey
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ESYT1/FAM62A
- 亚型
- IgG
- Top Product
- Discover our top product ESYT1 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
- ESYT1 (Extended Synaptotagmin-Like Protein 1 (ESYT1))
- 别名
- ESYT1/FAM62A (ESYT1 产品)
- 别名
- FAM62A antibody, fam62a antibody, si:ch211-239j9.4 antibody, DKFZp459I1628 antibody, MBC2 antibody, Fam62a antibody, Mbc2 antibody, vp115 antibody, extended synaptotagmin 1 antibody, extended synaptotagmin-like protein 1b antibody, extended synaptotagmin-like protein 1 antibody, ESYT1 antibody, esyt1b antibody, Esyt1 antibody
- 背景
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Synonyms: Extended synaptotagmin 1, KIAA0747, E Syt1, E-Syt1, Esyt1, ESYT1_HUMAN, Extended synaptotagmin like protein 1, Extended synaptotagmin-1, Family with sequence similarity 62 C2 domain containing member A, Family with sequence similarity 62 member A, MBC2, Membrane bound C2 domain containing protein, Membrane-bound C2 domain-containing protein, Protein FAM62A.
Background: Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy. The FAM62A gene product has been provisionally designated FAM62A pending further characterization.
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