GRAMD2 抗体 (AA 151-250) (FITC)
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- 抗原 See all GRAMD2 products
- GRAMD2 (GRAM Domain Containing 2 (GRAMD2))
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抗原表位
- AA 151-250
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适用
- 大鼠
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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 GRAMD2 antibody is conjugated to FITC
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse,Dog,Cow,Sheep,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GRAMD2
- 亚型
- IgG
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anti-GRAM Domain Containing 2 (GRAMD2) (AA 144-193) antibody
GRAMD2 适用: 人, 兔, 犬, 豚鼠, Bat, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-GRAM Domain Containing 2 (GRAMD2) (Middle Region) antibodyGRAMD2 适用: 人 WB 宿主: 兔 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
- GRAMD2 (GRAM Domain Containing 2 (GRAMD2))
- 别名
- GRAMD2 (GRAMD2 产品)
- 别名
- BC064463 antibody, RGD1564007 antibody, Gramd2 antibody, GRAM domain containing 2 antibody, GRAM domain containing 2A antibody, Gramd2 antibody, GRAMD2A antibody, Gramd2a antibody
- 背景
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Synonyms: GRAM domain containing 2, GRAM domain containing protein 2, GRAMD 2, GRAM2_HUMAN.
Background: GRAMD2 is a 354 amino acid single-pass membrane protein that contains one GRAM domain and is encoded by a gene that maps to human chromosome 15q23. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3 % of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
- 基因ID
- 196996
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