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OPA1 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)

OPA1 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 ABIN2727921
发货至: 中国
  • 抗原 See all OPA1 蛋白
    OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
    蛋白类型
    Recombinant
    产品特性
    Transcript Variant 3
    宿主
    • 6
    • 3
    资源
    • 6
    • 2
    • 1
    HEK-293 Cells
    标记
    This OPA1 protein is labelled with Myc-DYKDDDDK Tag.
    应用范围
    Antibody Production (AbP), Standard (STD)
    产品特性
    • Recombinant human Optic atrophy 1 (autosomal dominant) (OPA1), nuclear gene encoding mitochondrial protein, transcript variant 3 (transcript variant 3) 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 OPA1 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
    OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))
    Abstract
    OPA1 产品
    别名
    1200011N24Rik Protein, AI225888 Protein, AI847218 Protein, lilr3 Protein, mKIAA0567 Protein, MGM1 Protein, NPG Protein, NTG Protein, largeG Protein, fk62d06 Protein, wu:fb77a10 Protein, wu:fk62d06 Protein, zgc:92092 Protein, OPA1, mitochondrial dynamin like GTPase Protein, optic atrophy 1 (autosomal dominant) Protein, Opa1 Protein, OPA1 Protein, opa1 Protein
    背景
    This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene.
    分子量
    109.2 kDa
    NCBI登录号
    NP_570845
    途径
    Tube Formation
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