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ACP6 抗体

ACP6 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2430391
发货至: 中国
  • 抗原 See all ACP6 抗体
    ACP6 (Acid Phosphatase 6, Lysophosphatidic (ACP6))
    适用
    • 24
    • 7
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    宿主
    • 25
    • 2
    克隆类型
    • 27
    多克隆
    标记
    • 17
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ACP6 antibody is un-conjugated
    应用范围
    • 17
    • 7
    • 7
    • 3
    • 1
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human ACP6
    亚型
    IgG
    Top Product
    Discover our top product ACP6 Primary Antibody
  • 应用备注
    WB 1:500-1:2000, IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.2 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    储存液
    Sodium azide
    注意事项
    Avoid freeze / thaw cycles.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    ACP6 (Acid Phosphatase 6, Lysophosphatidic (ACP6))
    别名
    ACP6 (ACP6 产品)
    别名
    ACP6 antibody, im:7147584 antibody, zgc:172268 antibody, MGC146066 antibody, ACPL1 antibody, LPAP antibody, PACPL1 antibody, 5730559A09Rik antibody, AU022842 antibody, mPACPL1 antibody, acid phosphatase 6, lysophosphatidic antibody, acid phosphatase 6, lysophosphatidic S homeolog antibody, ACP6 antibody, acp6 antibody, acp6.S antibody, Acp6 antibody
    背景
    Lysophosphatidic acid phosphatase type 6 (ACP6), also designated acid phosphatase-like protein 1 (ACPL1) or lysophosphatidic acid phosphatase (LPAP), is a 428 amino acid secreted protein that hydrolyzes lysophosphatidic acid to monoacylglycerol. ACP6 is highly expressed in kidney, heart, small intestine, muscle, liver, prostate, testis, ovary and exists as two isoforms as a result of alternative splicing events. The gene encoding ACP6 maps to human chromosome 1, the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene of human chromosome 1, which encodes lamin A. Stickler syndrome, Parkinsons, Gaucher disease, familial adenomatous polyposis and Usher syndrome are also associated with chromosome 1. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
    分子量
    Calculated MW: 49 kDa
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