| 產(chǎn)品編號 | bs-4604R-BF488 |
| 英文名稱1 | Rabbit Anti-Leptin/BF488 Conjugated antibody |
| 中文名稱 | BF488標(biāo)記的瘦素抗體 |
| 別 名 | LEP; Leptin Murine Obesity Homolog; Leptin Precursor Obesity Factor; OB; Obese Protein; Obesity; Obesity factor; Obesity homolog mouse; Obesity Murine Homolog Leptin; OBS. |
| 規(guī)格價格 | 100ul/2980元 購買 大包裝/詢價 |
| 說 明 書 | 100ul |
| 研究領(lǐng)域 | 免疫學(xué) 生長因子和激素 糖尿病 |
| 抗體來源 | Rabbit |
| 克隆類型 | Polyclonal |
| 交叉反應(yīng) | (predicted: Human, Mouse, Rat, ) |
| 產(chǎn)品應(yīng)用 | IF=1:50-200
not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user. |
| 分 子 量 | 16kDa |
| 性 狀 | Lyophilized or Liquid |
| 濃 度 | 1mg/ml |
| 免 疫 原 | KLH conjugated synthetic peptide derived from human Leptin. |
| 亞 型 | IgG |
| 純化方法 | affinity purified by Protein A |
| 儲 存 液 | 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol |
| 保存條件 | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
| 產(chǎn)品介紹 |
background: Leptin, the product of the ob (obese) gene, is a 16kD protein consisting of 146 amino acid residues. Leptin is produced in the adipose tissue, and is considered to play an important role in appetite control, fat metabolism and regulation of body weight. It targets the central nervous system, particularly hypothalamus, affecting food intake. Leptin levels are high in most obese individuals. Studies have shown that it may also influence reproductive function. Function: May function as part of a signaling pathway that acts to regulate the size of the body fat depot. An increase in the level of LEP may act directly or indirectly on the CNS to inhibit food intake and/or regulate energy expenditure as part of a homeostatic mechanism to maintain constancy of the adipose mass. Subunit: Interacts with SIGLEC6. Subcellular Location: Secreted. DISEASE: Leptin deficiency (LEPD) [MIM:614962]: A rare disease characterized by low levels of serum leptin, severe hyperphagia and intractable obesity from an early age. Note=The disease is caused by mutations affecting the gene represented in this entry. Similarity: Belongs to the leptin family. Database links: Entrez Gene: 3952 Human Entrez Gene: 16846 Mouse Omim: 164160 Human SwissProt: P41159 Human SwissProt: P41160 Mouse Unigene: 194236 Human Unigene: 277072 Mouse Unigene: 44444 Rat Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. Leptin是一種分子量為16kDa的脂肪組織源激素，又稱：肥胖蛋白(Obese-protein)是由脂肪細(xì)胞分泌的，具有強(qiáng)親水性，以單體形式存在于血漿中。 Leptin 具有廣泛的生物學(xué)效應(yīng)，作用于下丘腦，調(diào)節(jié)食欲、能量代謝及體重。Leptin 還可能作為脂肪-胰島內(nèi)分泌軸的一部分，參與胰島素分泌的調(diào)節(jié)。 |
