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SMNDC1 抗体

SMNDC1 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN2458518
发货至: 中国
  • 抗原 See all SMNDC1 抗体
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    适用
    • 42
    • 25
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    • 5
    • 5
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    人, 小鼠, 大鼠
    宿主
    • 38
    • 5
    克隆类型
    • 40
    • 3
    多克隆
    标记
    • 22
    • 4
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    • 2
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    • 1
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    This SMNDC1 antibody is un-conjugated
    应用范围
    • 27
    • 19
    • 15
    • 6
    • 5
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB), ELISA
    纯化方法
    Antibody is purified by peptide affinity chromatography method.
    免疫原
    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SMNDC1.
    Top Product
    Discover our top product SMNDC1 Primary Antibody
  • 应用备注
    SMNDC1 antibody can be used for detection of SMNDC1 by ELISA at 1:1562500. SMNDC1 antibody can be used for detection of SMNDC1 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.
    浓度
    1 mg/mL
    缓冲液
    Antibody is lyophilized in PBS buffer with 2 % sucrose.
    注意事项
    As with any antibody avoid repeat freeze-thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    For short periods of storage (days) store at 4 °C. For longer periods of storage, store SMNDC1 antibody at -20 °C.
  • 抗原
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    别名
    SMNDC1 (SMNDC1 产品)
    别名
    smnr antibody, spf30 antibody, SMNDC1 antibody, SMNR antibody, SPF30 antibody, TDRD16C antibody, wu:fb37h07 antibody, wu:fc23a07 antibody, 2410004J23Rik antibody, 4933440I19Rik antibody, survival motor neuron domain containing 1 antibody, smndc1 antibody, SMNDC1 antibody, Bm1_41545 antibody, Smndc1 antibody
    背景
    This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. SMNDC1 is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.
    分子量
    27 kDa
    基因ID
    10285
    NCBI登录号
    NP_005862
    UniProt
    O75940
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