CEP152 抗体 (AA 901-1000)
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- 抗原 See all CEP152 抗体
- CEP152 (Centrosomal Protein 152kDa (CEP152))
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抗原表位
- AA 901-1000
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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 CEP152 antibody is un-conjugated
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应用范围
- ELISA, Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CEP152
- 亚型
- IgG
- Top Product
- Discover our top product CEP152 Primary Antibody
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anti-Centrosomal Protein 152kDa (CEP152) (Internal Region) antibody
CEP152 适用: 人 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Centrosomal Protein 152kDa (CEP152) (Internal Region) antibodyCEP152 适用: 人, 小鼠 ELISA, WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Centrosomal Protein 152kDa (CEP152) (C-Term) antibodyCEP152 适用: 人 ELISA, WB, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Centrosomal Protein 152kDa (CEP152) (AA 841-890) antibodyCEP152 适用: 人, 小鼠 ELISA, IHC 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
- 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
- CEP152 (Centrosomal Protein 152kDa (CEP152))
- 别名
- CEP152 (CEP152 产品)
- 别名
- AI851464 antibody, mKIAA0912 antibody, RGD1305348 antibody, MCPH4 antibody, MCPH9 antibody, SCKL5 antibody, centrosomal protein 152 antibody, CEP152 antibody, Cep152 antibody
- 背景
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Synonyms: CE152_HUMAN, Centrosomal protein 152 kDa, Centrosomal protein of 152 kDa, Cep152, FLJ21594, KIAA0912, MCPH4.
Background: Defects in CEP152 are the cause of microcephaly primary type 4 (MCPH4). A disease defined as a head circumference more than 3 standard deviations below the age-related mean. Brain weight is markedly reduced and the cerebral cortex is disproportionately small. Despite this marked reduction in size, the gyral pattern is relatively well preserved, with no major abnormality in cortical architecture. Affected individuals are mentally retarded. Primary microcephaly is further defined by the absence of other syndromic features or significant neurological deficits due to degenerative brain disorder.
- 基因ID
- 22995
- 途径
- M Phase
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