Kid Approved Rabbit Anti Human Tgfbi Polyclonal Antigen Affinity Purified (pbs With 0.05% Sodium Azide And 40% Glycerol, Ph7.4) (western Blot,ihc,elisa) Price Crushed By 35% [AKe4B96X]
Kid Approved Rabbit Anti Human Tgfbi Polyclonal Antigen Affinity Purified (pbs With 0.05% Sodium Azide And 40% Glycerol, Ph7.4) (western Blot,ihc,elisa) Price Crushed By 35% [AKe4B96X] from Innovative Research is a polyclonal antibody in a liquid format, buffered in PBS with 0.05% sodium azide
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Kid Approved Rabbit Anti Human Tgfbi Polyclonal Antigen Affinity Purified (pbs With 0.05% Sodium Azide And 40% Glycerol, Ph7.4) (western Blot,ihc,elisa) Price Crushed By 35% [AKe4B96X]
Kid Approved Rabbit Anti Human Tgfbi Polyclonal Antigen Affinity Purified (pbs With 0.05% Sodium Azide And 40% Glycerol, Ph7.4) (western Blot,ihc,elisa) Price Crushed By 35% [AKe4B96X] from Innovative Research is a polyclonal antibody in a liquid format, buffered in PBS with 0.05% sodium azide and 40% Glycerol, pH7.4 This antibody has been purified using Antigen Affinity Purified.
More Details:
- Host: Rabbit
- Species: Human, Mouse
- Target: TGFBI
- Clonality: Polyclonal
- Purity: Antigen Affinity Purified
- Immunogen: Fusion protein of human TGFBI
- Storage Conditions: Store at -20°C. Avoid freeze / thaw cycles.
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).
This product can be used in analytical tools such as Western Blot,IHC,ELISA.
At Innovative Research, we provide reliable, consistent products that deliver reliable, consistent results.
For research use only.
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