E-AB-18249
TGFBI Polyclonal Antibody
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£106.20
War £118.00
- SKU:
- E-AB-18249
- Zusätzliche Namen:
- >RGD containing collagen associated protein,AI181842,AI747162,BGH3,BIGH3,Beta ig,Beta ig h3,Beta ig-h3,Big h3,CDB1,CDG2,CDGG1,CSD,CSD1,CSD2,CSD3,EBMD,Kerato epithelin,Kerato-epithelin,LCD1,MGC150270,RGD CAP,RGD-CAP,RGD-containing collagen-associated prote
- Anwendung:
- IHC, WB
- Konzentration:
- 1.02 mg/ml
- Aufreinigung:
- Affinity Purified
- Lagerbedingungen:
- -20[o]C Avoid freeze/thaw cycles.
- Hersteller:
- Elabscience
- Host:
- Rabbit
- Reaktivitäten:
- Human, Mouse, Rat
- Buffer:
- Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
- Immunogen:
- Fusion protein of human TGFBI
- Uniprot:
- Q15582
- Synonyme:
- beta ig-h3;betaig-h3;BIGH3;CDB1;CDG2;CDGG1;CSD;CSD1;CSD2;CSD3;EBMD;kerato-epithelin;LCD1;RGD-CAP;RGD-containing collagen-associated protein;transforming growth factor beta-induced 68kDa;transforming growth factor-beta-induced protein ig-h3;transforming growth factor, beta-induced, 68kD
- Weitere Details:
- TGFBI,also named as BIGH3,Kerato-epithelin and RGD-CAP,binds to type I,II,and IV collagens. TGFBI is an adhesion protein which may play an important role in cell-collagen interactions. In cartilage,it may be involved in endochondral bone formation. TGFBI is an extracellular matrix adaptor protein,it has been reported to be differentially expressed in transformed tissues. TGFBI is a predictive factor of the response to chemotherapy,and suggest the use of TGFBI-derived peptides as possible therapeutic adjuvants for the enhancement of responses to chemotherapy. Defects in TGFBI are the cause of epithelial basement membrane corneal dystrophy (EBMD). Defects in TGFBI are the cause of corneal dystrophy Groenouw type 1 (CDGG1). Defects in TGFBI are the cause of corneal dystrophy lattice type 1 (CDL1). Defects in TGFBI are a cause of corneal dystrophy Thiel-Behnke type (CDTB). Defects in TGFBI are the cause of Reis-Buecklers corneal dystrophy (CDRB). Defects in TGFBI are the cause of lattice corneal dystrophy type 3A (CDL3A). Defects in TGFBI are the cause of Avellino corneal dystrophy (ACD).
- Versandbedingungen:
- Blue Ice