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SMNDC1 抗体 (Middle Region)

This anti-SMNDC1 antibody is a 兔 多克隆 antibody detecting SMNDC1 in WB 和 IHC. Suitable for 人, 小鼠, 大鼠, Cow, 犬, 兔, 豚鼠, 山羊, 马 和 斑马鱼.
产品编号 ABIN2778955
发货至: 中国

Quick Overview for SMNDC1 抗体 (Middle Region) (ABIN2778955)

抗原

See all SMNDC1 抗体
SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))

适用

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人, 小鼠, 大鼠, Cow, 犬, 兔, 豚鼠, 山羊, 马, 斑马鱼

宿主

  • 34
  • 5

克隆类型

  • 36
  • 3
多克隆

标记

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This SMNDC1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (IHC)
  • 抗原表位

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    Middle Region

    序列

    QFNNRAYSKN KKGQVKRSIF ASPESVTGKV GVGTCGIADK PMTQYQDTSK

    预测反应

    Cow: 100%, Dog: 100%, Goat: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 93%

    产品特性

    This is a rabbit polyclonal antibody against SMNDC1. It was validated on Western Blot using a cell lysate as a positive control.

    纯化方法

    Affinity Purified

    免疫原

    The immunogen is a synthetic peptide directed towards the middle region of human SMNDC1
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 238 AA

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    Lot specific

    缓冲液

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 抗原

    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))

    别名

    SMNDC1

    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.
    Alias Symbols: SMNR, SPF30
    Protein Interaction Partner: UBC, PRPF3, SF3B5, SND1, CUL3, SF3A2, ELAVL1, HIST3H3, mad2, KPNB1, SNRNP200, SNRPB, CDK5RAP3, PPAN, TSR1, RNMTL1, SF3B1, SF3B3, SF3B2, SF3A3, SF3B4, DDX21, RUVBL1, RPL3, FDFT1, EWSR1,
    Protein Size: 238

    分子量

    27 kDa

    基因ID

    10285

    NCBI登录号

    NM_005871, NP_005862

    UniProt

    O75940
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