货号 | AF4765 |
别名 | BTBTNbK14H9.2 (butyrophilin, subfamily 1, member A1); BTN; BTN1A1; butyrophilin subfamily 1 member A1; butyrophilin, subfamily 1, member A1 |
反应种属 | Mouse |
应用 | Western Blot(0.25 µg/mL) |
目标/特异性 | Detects mouse BTN1A1/Butyrophilin in direct ELISAs and Western blots. In direct ELISAs, approximately 25% cross-reactivity with recombinant human BTN1A1/Butyrophilin is observed. |
使用方法 | Western Blot: 0.25 µg/mL |
来源 | Reconstitute at 0.2 mg/mL in sterile PBS. |
产品组分 |
供应商 | R&D Systems |
Entrez Gene IDs | 696 (Human); 12231 (Mouse); 306956 (Rat) |
纯化方式 | Antigen Affinity-purified |
免疫原 | Mouse myeloma cell line NS0-derived recombinant mouse BTN1A1/Butyrophilin Ala27-Trp247 Accession # Q62556 |
生物活性 | Mouse |
标记 | Unconjugated |
溶解方法 | Reconstitute at 0.2 mg/mL in sterile PBS. |
背景 | Butyrophilin (Greek for “being like butter”; also Btn1a1) is a 66 kDa member of the BTN/MOG family of proteins. It is expressed on secretory mammary epithelium and associates with xanthine dehydrogenase. This is necessary for milk-lipid droplet secretion. Mature mouse Butyrophilin is 498 amino acids (aa) in length. It is a type I transmembrane glycoprotein that contains a 221 aa extracellular domain (ECD) (aa 27‑247) and a 256 aa cytoplasmic region. The ECD contains two V-type Ig‑like domains (aa 29‑141 and aa 149‑235). There are two potential splice variants. One shows a deletion of aa 145‑238, while a second shows a 36 aa substitution for aa 144‑524. Over aa 27‑247, mouse Butyrophilin shares 85% and 67% aa identity with rat and human Butyrophilin, respectively. |
运输条件 | Blue Ice |
存放说明 | -20℃ |
参考文献 |
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Detection of Mouse BTN1A1/Butyrophilin by Western Blot. Western blot shows lysates of mouse lactating mammary tissue. PVDF membrane was probed with 0.25 µg/mL of Sheep Anti-Mouse BTN1A1/Butyrophilin Antigen Affinity-purified Polyclonal Antibody (Catalog # AF4765) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). A specific band was detected for BTN1A1/Butyrophilin at approximately 66 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 8. |