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RDH12 抗体 (Middle Region)

Cited in 1 publication. This 兔 多克隆 anti-RDH12 antibody specifically detects RDH12 in WB. The antibody is reactive with 人, Pig, 大鼠 和 犬 samples.
产品编号 ABIN2785175
发货至: 中国
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Quick Overview for RDH12 抗体 (Middle Region) (ABIN2785175)

抗原

See all RDH12 抗体
RDH12 (Retinol Dehydrogenase 12 (All-Trans/9-Cis/11-Cis) (RDH12))

适用

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人, Pig, 大鼠, 犬

宿主

  • 14
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克隆类型

  • 15
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多克隆

标记

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This RDH12 antibody is un-conjugated

应用范围

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Western Blotting (WB)
  • 抗原表位

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    Middle Region

    序列

    HIGKIPFHDL QSEKRYSRGF AYCHSKLANV LFTRELAKRL QGTGVTTYAV

    预测反应

    Dog: 93%, Human: 100%, Pig: 79%, Rat: 79%

    产品特性

    This is a rabbit polyclonal antibody against RDH12. 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 RDH12
  • 应用备注

    Optimal working dilutions should be determined experimentally by the investigator.

    说明

    Antigen size: 316 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.
  • Sun, Gerth, Maeda, Lodowski, Van Der Kraak, Saperstein, Héon, Palczewski: "Novel RDH12 mutations associated with Leber congenital amaurosis and cone-rod dystrophy: biochemical and clinical evaluations." in: Vision research, Vol. 47, Issue 15, pp. 2055-66, (2007) (PubMed).

  • 抗原

    RDH12 (Retinol Dehydrogenase 12 (All-Trans/9-Cis/11-Cis) (RDH12))

    别名

    RDH12

    背景

    RDH12 is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. RDH12 also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 3 (LCA3).
    Alias Symbols: FLJ30273, LCA3, LCA13, SDR7C2
    Protein Interaction Partner: RBPMS, UBC, ANXA8L1, MAP1LC3A, BUB1,
    Protein Size: 316

    分子量

    35 kDa

    基因ID

    145226

    NCBI登录号

    NM_152443, NP_689656

    UniProt

    Q96NR8
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