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C1QL2/C1QTNF10补体C1q和肿瘤坏死因子相关蛋白10
点击次数：241发布时间：2012/12/3 20:39:09
更新日期：2024/9/5 14:42:48
所 在 地：中国大陆
产品型号：BY-9793R
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详细内容
货号：BY-9793R
英文名称：Anti-C1QL2/C1QTNF10
中文名称：补体C1q和肿瘤坏死因子相关蛋白10
其他名称：C1q ａnd tumor necrosis factor related protein 10;C1q domain containing protein;C1QL2;C1QL2_HUMAN;C1QTNF10;Complement C1q-like protein 2;Complement component 1, q subcomponent-like 2;CTRP10;gliacolin like.
抗体来源：Rabbit
克隆类型：polyclonal
蛋白分子量：predicted molecular weight: 30kDa
纯化方法：affinity purified by Protein A
交叉反应：hu, mo, rat
产品介绍：C1qL2, also known as CTRP10 or C1QTNF10, is a 287 amino acid secreted protein that contains one C1q domain ａnd one collagen-like domain. C1qL2 belongs to a large family of multimeric proteins with a signature globular domain homologous to C1QA. These proteins also share structural homology with TNF family members. The gene that encodes C1qL2 consists of approximately 2,653 bases ａnd maps to human chromosome 2q14.2. Consisting of 237 million bases, chromosome 2 encodes over 1,400 genes ａnd makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare ａnd morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 ａnd ABCG8. An extremely rare recessive genetic disorder, Alstr鰉 syndrome, is due to mutations in the ALMS1 gene.Subcellular Location : Secreted.
