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C1QL2 抗体 (Biotin)

C1QL2 适用: 人, 小鼠, 大鼠 WB, IHC (p) 宿主: 兔 Polyclonal Biotin
产品编号 ABIN1404703
发货至: 中国
  • 抗原 See all C1QL2 抗体
    C1QL2 (Complement Component 1, Q Subcomponent-Like 2 (C1QL2))
    适用
    • 27
    • 20
    • 17
    • 2
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 27
    • 1
    克隆类型
    • 27
    • 1
    多克隆
    标记
    • 9
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C1QL2 antibody is conjugated to Biotin
    应用范围
    • 21
    • 13
    • 4
    • 4
    • 2
    • 2
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    交叉反应
    人, 小鼠, 大鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human C1QL2/C1QTNF10
    亚型
    IgG
    Top Product
    Discover our top product C1QL2 Primary Antibody
  • 应用备注
    WB 1:300-5000
    IHC-P 1:200-400
    限制
    仅限研究用
  • 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
  • 抗原
    C1QL2 (Complement Component 1, Q Subcomponent-Like 2 (C1QL2))
    别名
    C1QTNF10 (C1QL2 产品)
    别名
    C1QTNF10 antibody, CTRP10 antibody, BC040774 antibody, complement C1q like 2 antibody, complement component 1, q subcomponent-like 2 antibody, C1ql2 antibody, C1QL2 antibody
    背景

    Synonyms: 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.

    Background: 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 syndrome, is due to mutations in the ALMS1 gene.

    基因ID
    165257
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