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GPR172B 抗体

GPR172B 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7239008
发货至: 中国
  • 抗原 See all GPR172B 抗体
    GPR172B (G Protein-Coupled Receptor 172B (GPR172B))
    适用
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    宿主
    • 35
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    克隆类型
    • 37
    多克隆
    标记
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    This GPR172B antibody is un-conjugated
    应用范围
    • 26
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    ELISA, Immunohistochemistry (IHC)
    产品特性
    Polyclonal Antibody
    纯化方法
    Affinity purification
    免疫原
    Synthetic peptide of human SLC52A1
    亚型
    IgG
    Top Product
    Discover our top product GPR172B Primary Antibody
  • 应用备注
    IHC 1:50-1:200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.8 mg/mL
    缓冲液
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    GPR172B (G Protein-Coupled Receptor 172B (GPR172B))
    别名
    GPR172B (GPR172B 产品)
    别名
    GPR172A antibody, MGC79729 antibody, GPR172B antibody, gpcr41 antibody, GPCR42 antibody, PAR2 antibody, RBFVD antibody, RFT1 antibody, RFVT1 antibody, hRFT1 antibody, Gpr172a antibody, Gpr172b antibody, RGD1560410 antibody, rRFT1 antibody, POPAR antibody, 2010003P03Rik antibody, D15Ertd747e antibody, mRFT1 antibody, solute carrier family 52 member 1 antibody, solute carrier family 52 member 2 antibody, solute carrier family 52 (riboflavin transporter), member 1 antibody, solute carrier family 52 (riboflavin transporter), member 1 L homeolog antibody, solute carrier protein 52, member 2 antibody, SLC52A1 antibody, SLC52A2 antibody, slc52a1 antibody, slc52a1.L antibody, Slc52a2 antibody
    背景
    Biological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. This gene encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same protein, have been identified.
    NCBI登录号
    NP_001098047
    UniProt
    Q9NWF4
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