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GPD1L 抗体 (AA 19-351)

The 兔 多克隆 anti-GPD1L antibody is suitable to detect GPD1L in samples from 人, 小鼠 和 大鼠. It has been validated for WB 和 ELISA.
产品编号 ABIN7994524
发货至: 中国
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Room 801-803
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for GPD1L 抗体 (AA 19-351) (ABIN7994524)

抗原

See all GPD1L 抗体
GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

适用

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  • 1
人, 小鼠, 大鼠

宿主

  • 36
  • 3

克隆类型

  • 38
  • 1
多克隆

标记

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  • 1
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This GPD1L antibody is un-conjugated

应用范围

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  • 17
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  • 11
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Western Blotting (WB), ELISA

质量等级

Carrier-free
  • 抗原表位

    • 11
    • 8
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    AA 19-351

    原理

    Anti-GPD1L Antibody

    特异性

    No cross reactivity with other proteins.

    交叉反应 (详细)

    No cross-reactivity with other proteins.

    产品特性

    Anti-GPD1L Antibody. Tested in ELISA, WB applications. This antibody reacts with Human, Mouse, Rat.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human GPD1L recombinant protein (Position: A19-T351).

    亚型

    IgG
  • 应用备注

    Western blot, 0.1-0.5 μg/mL, Human, Mouse, Rat ELISA, 0.1-0.5 μg/mL

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

    浓度

    500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    GPD1L (Glycerol-3-Phosphate Dehydrogenase 1-Like (GPD1L))

    别名

    GPD1L

    背景

    Background: GPD1L is a human gene. It is mapped to 3p22.3. The protein encoded by this gene contains a glycerol-3-phosphate dehydrogenase (NAD+) motif and shares 72 % sequence identity with GPD1. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).

    Gene Full Name: glycerol-3-phosphate dehydrogenase 1 like

    分子量

    35-40 kDa

    基因ID

    23171

    UniProt

    Q8N335
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