Human Prolactin / PRL Protein, Mouse IgG2a Fc Tag, low endotoxin

Proteins and Peptides

貨號 Cat. No.
PRN-H5257
規格 Size
1mg
品牌 Brand
ACROBiosystems
Species
Human
Conjugate
Unconjugated
Expression System
HEK293
Tag
Mouse IgG Fc Tag

Description




Source : 


Human Prolactin, Mouse IgG2a Fc Tag, low endotoxin (PRN-H5257) is expressed from human 293 cells (HEK293). It contains AA Leu 29 - Cys 227 (Accession # Q5THQ0-1).


 

Molecule : Prolactin


 

Synonyms : PRL,Prolactin


 

Format : Powder


 

Category : Cytokines&Growth Factors


 

Accession : NP_000939.1


 

Storage : -20℃


 

Shipping condition : Powder,RT


 

Molecular Weight : 49.8 kDa


 

Characteristics :


This protein carries a mouse IgG2a Fc tag at the C-terminus. The protein has a calculated MW of 49.8 kDa. The protein migrates as 50-55 kDa under reducing (R) condition (SDS-PAGE) due to glycosylation.


 

Endotoxin Level : Less than 0.1 EU per μg by the LAL method.


 

Buffer : Tris with Glycine, Arginine and NaCl, pH7.5


 

Description :


Prolactin (gene name PRL) is a secreted neuroendocrine pituitary hormone that acts primarily on the mammary gland to promote lactation, but has pleiotropic effects in both males and females. Prolactin is synthesized as a prohormone. Following cleavage of the signal peptide, the length of the mature hormone is between 194 and 199 amino acids, depending on species. Hormone structure is stabilized by three intramolecular disulfide bonds. Excessive secretion of prolactin - hyperprolactinemia - is a relative common disorder in humans. This condition has numerous causes, including prolactin-secreting tumors and therapy with certain drugs. The prolactin receptor (gene name PRLR) is a transmembrane type I glycoprotein that belongs to the cytokine hematopoietic receptor family. Expression of the prolactin receptor is widespread. Each prolactin molecule is thought to bind two receptor molecules


 

References :


(1) Farfel A., et al. 2018, Pediatr Endocrinol Rev.,15(3), 216-222. (2) De Mello-Coelho V., et al. 1998, Dev Immunol., 6(3-4), 317-23. (3) Wennbo H., et al. 2000, Oncogene., 19(8),1072-6.





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