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Solute Carrier Family 22 Member 5 (SLC22A5) (C-Term) Peptide

SLC22A5 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN983873
发货至: 中国
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Quick Overview for Solute Carrier Family 22 Member 5 (SLC22A5) (C-Term) Peptide (ABIN983873)

抗原

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

宿主

资源

  • 1
合成

应用范围

Blocking Peptide (BP), Western Blotting (WB)
  • 蛋白结构域

    C-Term

    序列

    GIVVPSTIFD PSELQDLSSK KQQSHNILDL LRTWNIRMVT IMSIMLWMTI

    产品特性

    This is a synthetic peptide designed for use in combination with anti-SLC22A5 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    纯化方法

    Purified
  • 应用备注

    Each Investigator should determine their own optimal working dilution for specific applications.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    浓度

    1 mg/mL

    缓冲液

    Final peptide concentration is 1 mg/mL in PBS.

    注意事项

    Avoid repeated freeze-thaw cycles.

    储存条件

    -20 °C

    储存方法

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原

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

    背景

    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.

    Alias Symbols: CDSP, FLJ46769, OCTN2, OCTN2VT

    Protein Interaction Partner: PDZD3,PDZK1,SLC9A3R1,SLC9A3R2

    Protein Size: 557

    分子量

    61 kDa

    基因ID

    6584

    NCBI登录号

    NM_003060, NP_003051

    UniProt

    O76082
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