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SLC22A5 抗体 (C-Term)

SLC22A5 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN3042852
发货至: 中国
  • 抗原 See all SLC22A5 抗体
    SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
    抗原表位
    • 4
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 531-547, C-Term
    适用
    • 25
    • 17
    • 14
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    小鼠, 大鼠
    宿主
    • 26
    克隆类型
    • 26
    多克隆
    标记
    • 16
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SLC22A5 antibody is un-conjugated
    应用范围
    • 14
    • 10
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    原理
    Rabbit IgG polyclonal antibody for Solute carrier family 22 member 5(SLC22A5) detection. Tested with WB in Mouse,Rat.
    序列
    KQWQIQSQTR MQKDGEE
    交叉反应 (详细)
    No cross reactivity with other proteins.
    产品特性
    Rabbit IgG polyclonal antibody for Solute carrier family 22 member 5(SLC22A5) detection. Tested with WB in Mouse,Rat.
    Gene Name: solute carrier family 22(organic cation/carnitine transporter), member 5
    Protein Name: Solute carrier family 22 member 5
    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(531-547aa KQWQIQSQTRMQKDGEE), different from the related rat sequence by two amino acids.
    亚型
    IgG
    Top Product
    Discover our top product SLC22A5 Primary Antibody
  • 应用备注
    WB: Concentration: 0.1-0.5 μg/mL, Tested Species: Mouse, Rat
    Notes: Tested Species: Species with positive results. Predicted Species: Species predicted to be fit for the product based on sequence similarities.
    Other applications have not been tested. Optimal dilutions should be determined by end users.
    说明

    Antibody can be supported by chemiluminescence kit ABIN921124 in WB.

    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 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Thimerosal, 0.05 mg Sodium azide.
    储存液
    Thimerosal (Merthiolate), Sodium azide
    注意事项
    This product contains Sodium azide and Thimerosal (Merthiolate): POISONOUS AND HAZARDOUS SUBSTANCES which should be handled by trained staff only.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    At -20°C for one year. After reconstitution, at 4°C for one month.
    It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
    有效期
    12 months
  • 抗原
    SLC22A5 (Solute Carrier Family 22 Member 5 (SLC22A5))
    别名
    SLC22A5 (SLC22A5 产品)
    别名
    CDSP antibody, OCTN2 antibody, OCTN2VT antibody, Lstpl antibody, Octn2 antibody, jvs antibody, slc22a5 antibody, MGC68932 antibody, CT1 antibody, UST2r antibody, ATOCT2 antibody, OCT2 antibody, ORGANIC CATION TRANSPORTER 2 antibody, YUP8H12R.2 antibody, YUP8H12R_2 antibody, organic cation/carnitine transporter 2 antibody, solute carrier family 22 member 5 antibody, solute carrier family 22 (organic cation transporter), member 5 antibody, solute carrier family 22 member 5 L homeolog antibody, organic cation/carnitine transporter 2 antibody, SLC22A5 antibody, Slc22a5 antibody, LOC100358417 antibody, slc22a5.L antibody, OCT2 antibody
    背景
    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.

    Synonyms: CDSP antibody|High-affinity sodium-dependent carnitine cotransporter antibody|OCTN2 antibody|OCTN2VT antibody|Organic cation/carnitine transporter 2 antibody|S22A5_HUMAN antibody|Slc22a5 antibody|Solute carrier family 22(organic cation/carnitine transporter) member 5 antibody|Solute carrier family 22 member 5 antibody
    UniProt
    Q9Z0E8
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