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AGRP rabbit pAb

Disease: Defects in AGRP may be a cause of autosomal dominant obesity [MIM: 601665]. Domain: The presence of a 'disulfide through disulfide knot' structurally defines this protein as a knottin. function: Plays a role in weight homeostasis. May play a role in the regulation of melanocortin receptors within the hypothalamus and adrenal gland, and therefore in the central control of feeding. similarity: Contains 1 agouti domain. tissue specificity: Expressed primarily in the adrenal gland, subthalamic nucleus, and hypothalamus, with a lower level of expression occurring in testis, lung, and kidney.

Product Specifications

Background

Disease:Defects in AGRP may be a cause of autosomal dominant obesity [MIM:601665]., domain:The presence of a 'disulfide through disulfide knot' structurally defines this protein as a knottin., function:Plays a role in weight homeostasis. May play a role in the regulation of melanocortin receptors within the hypothalamus and adrenal gland, and therefore in the central control of feeding., similarity:Contains 1 agouti domain., tissue specificity:Expressed primarily in the adrenal gland, subthalamic nucleus, and hypothalamus, with a lower level of expression occurring in testis, lung, and kidney.

UniProt

O00253

Swiss Prot

O00253

Reactivity

Human; Rat; Mouse

Immunogen

Synthesized peptide derived from human AGRP AA range: 21-70

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Concentration

1 mg/ml

Dilution

WB 1:1000-2000 ELISA 1:5000-20000

Storage Conditions

-20°C/1 year

Fragment

IgG

Subcellular Location

Secreted . Golgi apparatus lumen .

Other Product Names

Agouti-related protein

Gene ID (Human)

181

Available Sizes

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