C1QTNF2 抗体 (AA 101-200)
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- 抗原 See all C1QTNF2 products
- C1QTNF2 (C1q and Tumor Necrosis Factor Related Protein 2 (C1QTNF2))
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抗原表位
- AA 101-200
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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 C1QTNF2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Cow,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CTRP2
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- C1QTNF2 (C1q and Tumor Necrosis Factor Related Protein 2 (C1QTNF2))
- 别名
- CTRP2 (C1QTNF2 产品)
- 别名
- C1QTNF2 antibody, fe50b04 antibody, wu:fe50b04 antibody, CTRP2 antibody, zacrp2 antibody, 1810033K05Rik antibody, Ctrp2 antibody, RGD1561041 antibody, C1q and tumor necrosis factor related protein 2 antibody, C1q and TNF related 2 antibody, C1QTNF2 antibody, c1qtnf2 antibody, C1qtnf2 antibody
- 背景
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Synonyms: C1q and tumor necrosis factor related protein 2, C1QT2_HUMAN, C1qtnf2, Complement C1q tumor necrosis factor-related protein 2, CTRP2, Zacrp2.
Background: CTRP2 is a 285 amino acid secreted protein that contains one C1q domain and one collagen-like domain and is encoded by a gene that maps to human chromosome 5. Chromosome 5 contains 181 million base pairs and comprises nearly 6 % of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
- 基因ID
- 114898
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