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Recombinant Cat Interferon gamma Protein (His tag)

Recombinant Cat Interferon gamma Protein (His tag) (RMPP-00230815)

Cat. No.: RMPP-00230815

Category: Growth Factors & Cytokines

Research Area: Cardiovascular

INQUIRY 50 μg Customer Size

Product Features

Source E.coli
Purity > 97% SDS-PAGE. > 97% by HPLC.
Nature Recombinant
Animal Free No
Form Lyophilized
Applications SDS-PAGE; HPLC; Functional Studies
Key Features Expression system: E.coli; Purity: > 97% SDS-PAGE; Active: Yes; Suitable for: SDS-PAGE, HPLC, Functional Studies

Protein Information

UniProt ID O15520
Molecular Weight 20 kDa
Sequence QALGQDMVSPEATNSSSSSSSSSSSSSFSSPSSAGRHVRSYNHLQGDVRW RKLFSFTKYFLKIEKNGKVSGTKKENCPYSILEITSVEIGVVAVKAINSN YYLAMNKKGKLYGSKEFNNDCKLKERIEENGYNTYASFNWQHNGRQMYVA LNGKGAPRRGQKTRRKNTSAHFLPMVVHS
Sequence Similarities Belongs to the heparin-binding growth factors family.
Protein Length Full length protein
Cellular Localization Secreted.
Function Could be a growth factor active in the process of wound healing. Acts as a mitogen in the lung. May act in a manner similar to FGF-7.
Involvement in Disease Defects in FGF10 are the cause of autosomal dominant aplasia of lacrimal and salivary glands (ALSG). ALSG has variable expressivity, and affected individuals may have aplasia or hypoplasia of the lacrimal, parotid, submandibular and sublingual glands and absence of the lacrimal puncta. The disorder is characterized by irritable eyes, recurrent eye infections, epiphora (constant tearing) and xerostomia (dryness of the mouth), which increases the risk of dental erosion, dental caries, periodontal disease and oral infections.Defects in FGF10 are a cause of lacrimo-auriculo-dento-digital syndrome (LADDS); also known as Levy-Hollister syndrome. LADDS is a form of ectodermal dysplasia, a heterogeneous group of disorders due tothis product development of two or more ectodermal structures. LADDS is an autosomal dominant syndrome characterized by aplastic/hypoplastic lacrimal and salivary glands and ducts, cup-shaped ears, hearing loss, hypodontia and enamel hypoplasia, and distal limb segments anomalies. In addition to these cardinal features, facial dysmorphism, malformations of the kidney and respiratory system andthis product genitalia have been reported. Craniosynostosis and severe syndactyly are not observed.

Storage & Shipping

Shipping and Storage Shipped at 4°C. Store at +4°C short term (1-2 weeks). Store at -20°C long term. Avoid freeze / thaw cycle.
pH: 7.40Constituents: 5% Trehalose, 2.9% Sodium chloride, 0.24% Tris
This product is an active protein and may elicit a biological response in vivo, handle with caution.

For research use only. Not for clinical use.