GLCCI1 抗体 (AA 201-300) (Biotin)
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- 抗原 See all GLCCI1 抗体
- GLCCI1 (Glucocorticoid Induced Transcript 1 (GLCCI1))
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抗原表位
- AA 201-300
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适用
- 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 GLCCI1 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))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Sheep,Horse,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GLCCI1
- 亚型
- IgG
- Top Product
- Discover our top product GLCCI1 Primary Antibody
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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
- GLCCI1 (Glucocorticoid Induced Transcript 1 (GLCCI1))
- 别名
- GLCCI1 (GLCCI1 产品)
- 别名
- FAM117C antibody, GCTR antibody, GIG18 antibody, TSSN1 antibody, 2310047L21Rik antibody, A130036A18Rik antibody, Fam117c antibody, Gig18 antibody, Tssn1 antibody, sb:cb902 antibody, testhymin antibody, zgc:158237 antibody, RGD1563612 antibody, glucocorticoid induced 1 antibody, glucocorticoid induced transcript 1 antibody, glucocorticoid induced 1a antibody, glucocorticoid induced 1 L homeolog antibody, GLCCI1 antibody, Glcci1 antibody, glcci1a antibody, glcci1.L antibody
- 背景
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Synonyms: FAM117C, GIG18, GLCCI1, GLCI1_HUMAN, Glucocorticoid induced transcript 1, Glucocorticoid-induced transcript 1 protein, TSSN1.
Background: GLCCI1, also known as TSSN1, GIG18 or FAM117C, is a 547 amino acid protein found in thymus and CD4(+)CD8(+) cells during specific stages of spermatogenesis in testis. Subject to phosphorylation, GLCCI1 is encoded by a gene located on human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
- 基因ID
- 113263
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