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SRP3171

Sigma-Aldrich

TGF-beta 3-E. coli human

recombinant, expressed in E. coli, ≥98% (SDS-PAGE), ≥98% (HPLC), suitable for cell culture

Sinonimo/i:

Transforming Growth Factor-beta3

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10 μG
CHF 366.00

CHF 366.00


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10 μG
CHF 366.00

About This Item

Codice UNSPSC:
12352202
NACRES:
NA.32

CHF 366.00


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Origine biologica

human

Ricombinante

expressed in E. coli

Saggio

≥98% (HPLC)
≥98% (SDS-PAGE)

Stato

lyophilized

Potenza

≤0.05 ng/mL ED50

PM

25.0 kDa

Confezionamento

pkg of 10 μg

tecniche

cell culture | mammalian: suitable

Impurezze

<0.1 EU/μg endotoxin, tested

Colore

white

N° accesso UniProt

Condizioni di spedizione

wet ice

Temperatura di conservazione

−20°C

Informazioni sul gene

human ... TGFB3(7043)

Descrizione generale

The gene TGF-β3 (transforming growth factor β 3) is mapped to human chromosome 14q24.3.[1] The three mammalian isoforms of TGF-β, TGF-β1, β2, β3 elicit similar biological responses.[2] TGF-β proteins are made as precursor molecules which are cut to generate a mature carboxy-terminal region of 110-140 amino acids.[3] They are secreted predominantly as latent complexes which are stored at the cell surface and in the extracellular matrix. The release of biologically active TGF-β isoform from a latent complex involves proteolytic processing of the complex and/or induction of conformational changes by proteins such as thrombospondin-1.[3][4] Recombinant TGF-β3 is a 25.0kDa protein composed of two identical 112 amino acid polypeptide chains linked by a single disulfide bond.

Applicazioni

TGF-β3 (transforming growth factor β 3) human has been used in the media for the chondrogenic differentiation of the stromal cells.[5][6] It has been used in the culture medium to allow attachment of primary human dermal fibroblasts to the scaffolds.[7]

Azioni biochim/fisiol

The three mammalian isoforms of TGF-β (transforming growth factor β), TGF-β1, β2, β3, are multifunctional cytokines that regulate cell proliferation, growth, differentiation and motility as well as synthesis and deposition of the extracellular matrix. They are involved in various physiological processes including embryogenesis, tissue remodeling and wound healing.[3] TGF-β3 is the predominant TGF-β in the testis and controls the blood-testis barrier activity. Polymorphisms in this gene might be associated with male infertility.[8] Heterozygous mutation in the gene at position Arg300 might be associated with increased TGF-β signaling, leading to a disorder with phenotypic overlap with Marfan syndrome and Loeys-Dietz syndrome.[9] TGF-β3 is involved in the mesenchymal stem cells (MSCs)-mediated inhibition of fibroblast proliferation and decreases skin fibrosis.[10]

Sequenza

ALDTNYCFRN LEENCCVRPL YIDFRQDLGW KWVHEPKGYY ANFCSGPCPY LRSADTTHST VLGLYNTLNP EASASPCCVP QDLEPLTILY YVGRTPKVEQ LSNMVVKSCK CS

Stato fisico

Lyophilized from 0.1% TFA

Ricostituzione

Centrifuge the vial prior to opening. Reconstitute in water to a concentration of 0.1- 1.0 mg/ml. Do not vortex. This solution can be stored at 2-8 °C for up to 1 week. For extended storage, it is recommended to further dilute in a buffer containing a carrier protein (example 0.1% BSA) and store in working aliquots at -20 °C to -80 °C.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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The TGF-beta superfamily: new members, new receptors, and new genetic tests of function in different organisms.
Kingsley DM
Genes & Development, 8, 133-146 (1994)
A comparison study of different physical treatments on cartilage matrix derived porous scaffolds for tissue engineering applications.
Science and Technology of Advanced Materials (2016)
Transforming growth factor-beta(1), -beta(2), -beta(3), basic fibroblast growth factor and vascular endothelial growth factor expression in keratinocytes of burn scars.
Hakvoort T
European Cytokine Network, 11, 233-239 (2000)
Association between TGFB3 and nonsyndromic cleft lip with or without cleft palate in a Chilean population.
Suazo J
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association, 47, 513-517 (2010)
Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome.
Kuechler A
Molecular and Cellular Probes, 29, 330-334 (2015)

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