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ACP2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

ACP2 宿主: 人 宿主: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
产品编号 ABIN2714336
发货至: 中国
  • 抗原 See all ACP2 蛋白
    ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 1
    宿主
    • 4
    • 4
    资源
    • 4
    • 3
    • 1
    HEK-293 Cells
    标记
    This ACP2 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human ACP2 / LAP (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product ACP2 蛋白
  • 应用备注
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    说明

    The tag is located at the C-terminal.

    限制
    仅限研究用
  • 浓度
    50 μg/mL
    缓冲液
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    储存条件
    -80 °C
    储存方法
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • 抗原
    ACP2 (Acid Phosphatase 2, Lysosomal (ACP2))
    别名
    Acp2,lap (ACP2 产品)
    别名
    ACP2 Protein, Acp-2 Protein, LAP Protein, acid phosphatase 2, lysosomal Protein, acid phosphatase 2, lysosomal S homeolog Protein, ACP2 Protein, acp2 Protein, Acp2 Protein, acp2.S Protein
    背景
    This gene encodes the beta subunit of lysosomal acid phosphatase (LAP). LAP is chemically and genetically distinct from red cell acid phosphatase. The encoded protein belongs to a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. LAP-deficiencies in mice cause multiple defects including bone structure alterations, lysosomal storage defects in the kidneys and central nervous system, and an increased tendency towards seizures. An enzymatically-inactive allele of LAP in mice exhibited a more severe phenotype than the null allele, and defects included cerebellum abnormalities, growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternative splicing results in multiple transcript variants encoding different isoforms.
    分子量
    45.1 kDa
    NCBI登录号
    NP_001601
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