SLC17A1 | NPT1 Rabbit pAb(bs-19800R)-50ul/100ul/200ul产品图

SLC17A1 | NPT1 Rabbit pAb(bs-1

9800R)-50ul/100ul/200ul
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  • ￥1180 - 2800
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  • bs-19800R
  • 2026年10月13日
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    北京博奥森生物技术有限公司
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      50ul/100ul/200ul

    规格：50ul产品价格：￥1180.0
    规格：100ul产品价格：￥1980.0
    规格：200ul产品价格：￥2800.0
    产品编号bs-19800R
    英文名称SLC17A1 Rabbit pAb
    中文名称溶质载体家族蛋白17成员A1抗体
    英文别名Na(+)/PI cotransporter 1; Na/Pi-4; NAP 1; Napi1; NPT 1; Npt1; NPT1_HUMAN; Renal Na(+)-dependent phosphate cotransporter 1; Renal sodium-dependent phosphate transport protein 1; Renal sodium-phosphate transport protein 1; Slc17a1; Sodium phosphate transporter; Sodium-dependent phosphate transport protein 1; Sodium/phosphate cotransporter 1; Sodium/phosphate type I cotransporter; Solute carrier family 17(organic anion transporter) member 1; solute carrier family 17(sodium phosphate), member 1; Solute carrier family 17(vesicular glutamate transporter) member 1; Solute carrier family 17 member 1.
    产品应用IHC-P=1:100-500, IHC-F=1:100-500, ICC/IF=1:100-500, IF=1:100-500, ELISA=1:5000-10000

    Not yet tested in other applications.
    Optimal working dilutions must be determined by the end user.

    交叉反应 (Human, Mouse, Rat)
    抗体来源Rabbit
    免疫原KLH conjugated synthetic peptide derived from human SLC17A1
    亚型IgG
    性状Liquid
    纯化方法affinity purified by Protein A
    克隆类型Polyclonal
    理论分子量51 kDa
    浓度1mg/ml
    储存液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    研究领域

    Signal Transduction > Metabolism > Plasma Membrane > Channels

    亚细胞定位Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A soluble form: Secreted (By similarity).
    组织特异性Expressed at very low levels in all tissues tested.
    相似性Belongs to the glycosyltransferase 54 family.
    功能May be a carrier that transport small solutes by using chemiosmotic ion gradients
    保存条件Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事项This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    背景资料MFSD8 is a 518 amino acid multi-pass membrane protein of the lysosome that is thought to function as a carrier protein that transports small solutes by way of chemiosmotic ion gradients. Expressed at low levels in many tissues, MFSD8 is encoded by a gene that maps to human chromosome 4q28.1. Defects in the gene encoding MFSD8 are the cause of a late infantile neuronal ceroid lipofuscinosis known as neuronal ceroid lipofuscinosis type 7 (CLN7). CLN7 is characterized by seizures, progressive dementia and visual failure.

     

    应用推荐稀释比例
    {IHC-P}{1:100-500}
    {IHC-F}{1:100-500}
    {ICC/IF}{1:100-500}
    {IF}{1:100-500}
    {ELISA}{1:5000-10000}

     

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