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Leptin Rabbit pAb (bs-10888R)  
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產品編號 bs-10888R
英文名稱 Leptin Rabbit pAb
中文名稱 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; LEP_HUMAN.  
研究領域 心血管  神經生物學  信號轉導  干細胞  生長因子和激素  糖尿病  新陳代謝  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Human (predicted: Mouse,Rat)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 16 kDa
檢測分子量
細胞定位 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 Recombinant human Leptin: 22-167/167 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 This gene encodes a protein that is secreted by white adipocytes, and which plays a major role in the regulation of body weight. This protein, which acts through the leptin receptor, functions as part of a signaling pathway that can inhibit food intake and/or regulate energy expenditure to maintain constancy of the adipose mass. This protein also has several endocrine functions, and is involved in the regulation of immune and inflammatory responses, hematopoiesis, angiogenesis and wound healing. Mutations in this gene and/or its regulatory regions cause severe obesity, and morbid obesity with hypogonadism. This gene has also been linked to type 2 diabetes mellitus development. [provided by RefSeq, Jul 2008].

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 (Probable).

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.

SWISS:
P41159

Gene ID:
3952

Database links:

Entrez Gene: 3952 Human

Entrez Gene: 16846 Mouse

Entrez Gene: 25608 Rat

Omim: 164160 Human

SwissProt: P41159 Human

SwissProt: P41160 Mouse

SwissProt: Q29406 Pig

SwissProt: P50596 Rat

SwissProt: Q28603 Sheep

Unigene: 194236 Human

Unigene: 277072 Mouse

Unigene: 44444 Rat



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)是由脂肪細胞分泌的,具有強親水性,以單體形式存在于血漿中。 Leptin 具有廣泛的生物學效應,作用于下丘腦,調節食欲、能量代謝及體重。Leptin 還可能作為脂肪-胰島內分泌軸的一部分,參與胰島素分泌的調節。
產品圖片
Sample: Lane 1: Recombinant human Leptin, C-His(bs-10888P) Primary: Anti-Leptin (bs-10888R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 16 kDa Observed band size: 16 kDa
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