Overblog Alle Blogs
Edit post Folge diesem Blog Administration + Create my blog
MENU

Mein Blog umfasst die aktuellesten News, Forschungsleistung, neuesten Produkte und Service von Sino Biological Inc. und die aktuelle News von Life Sciences. Sie können sich hier wissenschaftlich informieren.Willkommen zu meinem Blog.Viel Spaß!

Werbung

MAPK14 / p38 alpha Protein (His Tag)

Sino Biological Inc. liefert MAPK14 / p38 alpha Protein (His Tag) mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über MAPK14 / p38 alpha Protein (His Tag) lesen Sie bitte: http://www.sinobiological.com/MAPK14-p38-alpha-Protein-g-9934.html

Produkt-Information von MAPK14 / p38 alpha Protein

Synonym MAPK14, CSBP, CSBP1, CSBP2, CSPB1, MXI2, SAPK2A
Protein Construction

A DNA sequence encoding the human MAPK14 (P63098)(Met1-Ser360) was fused with a polyhistide tag at the N-terminus.

Source Human
Expression Host Baculovirus-Insect cells

QC Testing von MAPK14 / p38 alpha Protein

Purity > 90% as determined by SDS-PAGE SDS-PAGE:
SDS-PAGE

MAPK14 protein

Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method
Stability Samples are stable for up to twelve months from date of receipt at -70℃
Predicted N terminal His
Molecular Mass

The recombinant human MAPK14 consists of 378 amino acids and has a calculated molecular mass of  43.7 kDa. The recombinant protein migrates as an approximately 43 kDa band in SDS-PAGE under reducing conditions.

Formulation Lyophilized from sterile 20mM Tris, 500mM NaCl, pH7.4, 10%gly.
  1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.

Usage Guide von MAPK14 / p38 alpha Protein

Storage Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

Verwandte Produkte & Themen von MAPK14 / p38 alpha Protein

Related Areas:

Enzyme>>Protein Kinase>>Intracellular Kinase>>p38 alpha/MAPK14

Signal Transduction>>Protein Kinase>>Intracellular Kinase>>p38 alpha/MAPK14

Proteins:
Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
p38 alpha/MAPK14 Human MAPK14 / p38 alpha Protein, Recombinant 10081-H07B
p38 alpha/MAPK14 Human p38 alpha/MAPK14 Protein, Recombinant 10081-H08B
p38 alpha/MAPK14 Human p38 alpha/MAPK14 Protein, Recombinant 10646-H07B
p38 alpha/MAPK14 Human p38 alpha/MAPK148 Protein, Recombinant 10646-HNCB
Antibodies:

Beschreibung von MAPK14 / p38 alpha Protein

Mitogen-activated protein (MAP) kinases are intracellular serine/threonine kinases activated by dual phosphorylation of adjacent threonine and tyrosine, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. Human p38 MAP kinase, also known as MAPK14, is activated following exposure to products of microbial pathogens, physical-chemical stimuli and cytokines. Either its autophosphorylation triggered by the interaction with MAP3K7IP1/TAB1 protein, or phosphorylation by MAP kinase kinases (MKKs) is requisite for activation of MAPK14/p38 alpha. It transduces signals by phosphorylating a number of downstream molecules including transcription factors ATF2, MEF2C, and MAX, cell cycle regulator CDC25B, as well as tumor suppressor p53. p38 thus exists as an important regulator of both embryonic development and cancer progression. Four alternatively spliced transcript variants have been reported, and MAPK14/p38 alpha of 360 amino acids is the best characterized isoform. Furthermore, the MAPK14/p38 alpha has been suggested to play a critical role linking developmental and stress-induced erythropoiesis through regulation of Epo expression.

References

  1. Han J. et al., 1995, Biochim Biophys Acta. 1265: 224-7.
  2. Ben-Levy R. et al., 1998, Curr Biol. 8: 1049-57.
  3. Tamura K. et al., 2000, Cell. 102: 221-31.
  4. Bradham C. et al., 2006, Cell Cycle. 5: 824-8.
Werbung
Zurück zu Home
Diesen Post teilen
Repost0
Um über die neuesten Artikel informiert zu werden, abonnieren:
Kommentiere diesen Post