GLCCI1 抗体 (AA 201-300) (Cy7)
Quick Overview for GLCCI1 抗体 (AA 201-300) (Cy7) (ABIN1416794)
抗原
See all GLCCI1 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 201-300
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交叉反应
- 小鼠
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预测反应
- Human,Rat,Dog,Cow,Sheep,Horse,Chicken
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human GLCCI1
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亚型
- IgG
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anti-Glucocorticoid Induced Transcript 1 (GLCCI1) antibody
GLCCI1 适用: 人, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Glucocorticoid Induced Transcript 1 (GLCCI1) (AA 255-304) antibodyGLCCI1 适用: 人, 小鼠, Cow, 马, Pig, 大鼠, 兔, 小鸡 WB 宿主: 兔 Polyclonal unconjugated
anti-Glucocorticoid Induced Transcript 1 (GLCCI1) (AA 179-228) antibodyGLCCI1 适用: 人, 小鼠, Cow, 马, Pig, 大鼠, 犬, 小鸡, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Glucocorticoid Induced Transcript 1 (GLCCI1) (AA 226-255) antibodyGLCCI1 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB32643 unconjugated
anti-Glucocorticoid Induced Transcript 1 (GLCCI1) (Middle Region) antibodyGLCCI1 适用: 人, 小鼠, Cow, 马, Pig, 大鼠, 兔, 犬, 豚鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Glucocorticoid Induced Transcript 1 (GLCCI1) (AA 233-263), (Middle Region) antibodyGLCCI1 适用: 人 WB, IHC (p), EIA 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
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- GLCCI1 (Glucocorticoid Induced Transcript 1 (GLCCI1))
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别名
- GLCCI1
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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.
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基因ID
- 113263
抗原
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