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SLC22A5 抗体 (C-Term) (HRP)

The HRP-conjugated 兔 多克隆 anti-SLC22A5 antibody (ABIN8039578) specifically detects SLC22A5 in WB, ELISA 和 IHC. The antibody is reactive with 小鼠 和 大鼠 samples.
产品编号 ABIN8039578
发货至: 中国
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Quick Overview for SLC22A5 抗体 (C-Term) (HRP) (ABIN8039578)

抗原

See all SLC22A5 抗体
SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))

适用

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小鼠, 大鼠

宿主

  • 38

克隆类型

  • 38
多克隆

标记

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This SLC22A5 antibody is conjugated to HRP

应用范围

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

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    C-Term

    原理

    Anti-Solute carrier family 22 member 5/SLC22A5 Antibody HRP Conjugated

    特异性

    No cross reactivity with other proteins.

    交叉反应 (详细)

    No cross-reactivity with other proteins

    预测反应

    different from the related rat sequence by two amino acids.

    纯化方法

    Immunogen affinity purified.

    免疫原

    A synthetic peptide corresponding to a sequence at the C-terminus of mouse Solute carrier family 22 member 5, different from the related rat sequence by two amino acids.

    亚型

    IgG
  • 应用备注

    Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

    有效期

    12 months
  • 抗原

    SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))

    别名

    SLC22A5

    背景

    Background: Solute carrier family 22 (organic cation/carnitine transporter), member 5, also called SLC22A5 or OCTN2 is a membrane transport protein associated with primary carnitine deficiency. This gene is mapped to 5q31.1. Polyspecific organic cation transporters in the liver, kidney, intestine, and other organs are critical for elimination of many endogenous small organic cations as well as a wide array of drugs and environmental toxins. The encoded protein is a plasma integral membrane protein which functions both as an organic cation transporter and as a sodium-dependent high affinity carnitine transporter. The encoded protein is involved in the active cellular uptake of carnitine. Mutations in this gene are the cause of systemic primary carnitine deficiency (CDSP), an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation, and later in life by skeletal myopathy or cardiomyopathy.

    Gene Full Name: solute carrier family 22 (organic cation transporter), member 5

    基因ID

    20520

    UniProt

    Q9Z0E8
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