GIDRP88 抗体 (AA 641-740) (Biotin)
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- 抗原 See all GIDRP88 (C10orf28) products
- GIDRP88 (C10orf28) (Chromosome 10 Open Reading Frame 28 (C10orf28))
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抗原表位
- AA 641-740
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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 GIDRP88 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GIDRP88
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 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
- 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- GIDRP88 (C10orf28) (Chromosome 10 Open Reading Frame 28 (C10orf28))
- 别名
- GIDRP88 (C10orf28 产品)
- 别名
- 1700036B12Rik antibody, AI450607 antibody, C10orf28 antibody, D19Ertd386e antibody, GIDRP86 antibody, Gidrp88 antibody, GIDRP88 antibody, PSORT antibody, R3H domain and coiled-coil containing 1 like antibody, R3hcc1l antibody, R3HCC1L antibody
- 背景
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Synonyms: GIDRP86, C10orf28, Chromosome 10 open reading frame 28, FLJ25458, FLJ37160, Growth inhibition and dferentiation related protein 86, PSORT, Putative mitochondrial space protein 32.1, R3HCL_HUMAN.
Background: C10orf28 is a 792 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding C10orf28 maps to human chromosome 10, which spans nearly 135 million base pairs, makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
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