C1QL2 抗体 (AA 200-280)
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Quick Overview for C1QL2 抗体 (AA 200-280) (ABIN7213882)
抗原
See all C1QL2 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 200-280
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原理
- C1qL2 Polyclonal Antibody
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特异性
- C1qL2 Polyclonal Antibody detects endogenous levels of C1qL2 protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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免疫原
- Synthesized peptide derived from the C-terminal region of human C1qL2 at AA range: 200-280
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亚型
- IgG
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应用备注
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:10000). Not yet tested in other applications.
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说明
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Primary Antibody
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: 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
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- C1QL2 (Complement Component 1, Q Subcomponent-Like 2 (C1QL2))
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别名
- C1qL2
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背景
- Rabbit Anti-C1qL2 Polyclonal Antibody,C1QL2, Complement C1q-like protein 2,C1qL2 (complement C1q-like protein 2), 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, Alström syndrome, is due to mutations in the ALMS1 gene.,Complement C1q-like protein 2
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分子量
- observerd band 32-36kDa
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基因ID
- 165257
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UniProt
- Q7Z5L3
抗原
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