GCM2 抗体 (AA 61-160) (Cy5)
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- 抗原 See all GCM2 抗体
- GCM2 (Glial Cells Missing Homolog 2 (GCM2))
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抗原表位
- AA 61-160
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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 GCM2 antibody is conjugated to Cy5
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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,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GCM2
- 亚型
- IgG
- Top Product
- Discover our top product GCM2 Primary Antibody
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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
- GCM2 (Glial Cells Missing Homolog 2 (GCM2))
- 别名
- GCM2 (GCM2 产品)
- 别名
- GCMb antibody, Gcm-2 antibody, gcm-2 antibody, GCMB antibody, hGCMb antibody, Gcm-rs1 antibody, Gcm1 antibody, Gcm1-rs2 antibody, glial cells missing homolog 2 antibody, glial cells missing homolog 2 (Drosophila) antibody, glial cells missing homolog 2 S homeolog antibody, GCM2 antibody, gcm2 antibody, gcm2.S antibody, Gcm2 antibody
- 背景
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Synonyms: Chorion-specic transcription factor GCMb, GCM mot protein 2, GCMb, Glial cells missing homolog 2, glial cells missing homolog b, GCM2_HUMAN.
Background: Glial cells missing homolog 2 (GCM2), also known as Chorion-specific transcription factor GCMb, is a 506 amino acid nuclear protein. GCM2 is a transcription factor that acts as an essential regulator of parathyroid development. GCM2 is also thought to mediate the effect of calcium on parathyroid hormone expression and secretion in parathyroid cells. GCM2 contains one N-terminal GCM domain, which has DNA binding activity. Mutations of the gene that encodes GCM2 are associated with hypoparathyroidism, an autosomal recessive condition characterized by hypocalcemia and hyperphosphatemia.
- 基因ID
- 9247
- UniProt
- O75603
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