ARG64270

anti-TPD52 antibody

anti-TPD52 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Cancer antibody; Immune System antibody

概述

产品描述 Goat Polyclonal antibody recognizes TPD52
反应物种 Hu
应用 IHC-P, WB
特异性 This antibody is expected to recognise all three reported isoforms (NP_001020423.1, NP_001020424.1and NP_005070.1).
宿主 Goat
克隆 Polyclonal
同位型 IgG
靶点名称 TPD52
抗原物种 Human
抗原 C-TEPLPEKTQES
偶联标记 Un-conjugated
別名 PrLZ; Tumor protein D52; PC-1; Protein N8; hD52; N8L; D52

应用说明

应用建议
应用 推荐稀释比
IHC-P3 - 5 µg/ml
WB1 - 3 µg/ml
应用说明 WB: Recommend incubate at RT for 1h.
IHC-P: Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0).
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

属性

形式 Liquid
纯化 Purified from goat serum by antigen affinity chromatography.
缓冲液 Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA.
抗菌剂 0.02% Sodium azide
稳定剂 0.5% BSA
浓度 0.5 mg/ml
存放说明 For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项 For laboratory research only, not for drug, diagnostic or other use.

生物信息

数据库连接

GeneID: 7163 Human TPD52

Swiss-port # P55327 Human Tumor protein D52

基因名称 TPD52
全名 tumor protein D52
研究领域 Cancer antibody; Immune System antibody
预测分子量 24 kDa

检测图片 (2) Click the Picture to Zoom In

  • ARG64270 anti-TPD52 antibody WB image

    Western Blot: Human Lymph Node lysate (35 µg protein in RIPA buffer) stained with ARG64270 anti-TPD52 antibody at 1 µg/ml dilution.

  • ARG64270 anti-TPD52 antibody IHC-P image

    Immunohistochemistry: Paraffin-embedded Human spleen tissue. Antigen Retrieval: Steam tissue section in Citrate buffer (pH 6.0). The tissue section was stained with ARG64270 anti-TPD52 antibody at 3.75 µg/ml dilution followed by AP-staining.