电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

PMPCA Protein (Myc-DYKDDDDK Tag)

PMPCA 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 ABIN2729218
发货至: 中国
  • 抗原 See all PMPCA products
    PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))
    蛋白类型
    Recombinant
    宿主
    • 2
    • 1
    • 1
    • 1
    资源
    • 2
    • 2
    • 1
    HEK-293 Cells
    标记
    This PMPCA protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human PMPCA protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    纯度
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
  • 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
    PMPCA (Peptidase (Mitochondrial Processing) alpha (PMPCA))
    别名
    Pmpca (PMPCA 产品)
    别名
    Alpha-MPP Protein, INPP5E Protein, 1200002L24Rik Protein, 4933435E07Rik Protein, P-55 Protein, wu:fi19e06 Protein, wu:fj83d11 Protein, zgc:101647 Protein, MGC114896 Protein, DKFZp459H0315 Protein, peptidase, mitochondrial processing alpha subunit Protein, peptidase (mitochondrial processing) alpha Protein, peptidase (mitochondrial processing) alpha S homeolog Protein, PMPCA Protein, Pmpca Protein, pmpca Protein, pmpca.S Protein
    背景
    The protein encoded by this gene is found in the mitochondrion, where it represents the alpha subunit of a proteolytic heterodimer. This heterodimer is responsible for cleaving the transit peptide from nuclear-encoded mitochondrial proteins. Defects in this gene are a cause of spinocerebellar ataxia, autosomal recessive 2.
    分子量
    58.1 kDa
    NCBI登录号
    NP_055975
    途径
    Inositol Metabolic Process, SARS-CoV-2 Protein Interactome
You are here:
客服