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Antibodies

Recombinant Vitronectin/S-Protein Monoclonal Antibody

Product Sizes
50 ul
£281.00
AN301686L-50UL
100 ul
£402.00
AN301686L-100UL
About this Product
SKU:
AN301686L
Additional Names:
VTN;V75;VN;VNT;Complement S Protein;Epibolin;S Protein;Serum Spreading Factor;Serum-spreading factor;Somatomedin B;Somatomedin-B;S-protein;Vitronectin V10 subunit;Vitronectin V65 subunit;VTNC;Complement S-protein;Vitronectin
Application:
Flow Cytometry, Immunofluorescence, Immunohistochemistry, Western Blot
Buffer:
PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
translate.label.attr.clone:
A389
Clonality:
Recombinant Monoclonal
Concentration:
1 mg/ml
Extra Details:
Vitronectin is a cell adhesion and spreading factor found in serum and tissues. Vitronectin interact with glycosaminoglycans and proteoglycans. Is recognized by certain members of the integrin family and serves as a cell-to-substrate adhesion molecule. Inhibitor of the membrane-damaging effect of the terminal cytolytic complement pathway.
Host:
Rabbit
Immunogen:
Recombinant human Vitronectin/S-Protein fragment
Isotype:
IgG, kappa
Purification:
Protein A Purified
Reactivities:
Human
Shipping Conditions:
Blue Ice
Storage Conditions:
-20[o]C Avoid freeze/thaw cycles.
Supplier:
Elabscience
Type:
Antibody: Recombinant Antibodies
Western Blot with Vitronectin/S-Protein Monoclonal Antibody at dilution of 1:2000. Lane 1: Human serum
Immunohistochemistry of paraffin-embedded Human liver using Vitronectin/S-Protein Monoclonal Antibody at dilution of 1:100.
Immunofluorescent analysis of (4% Paraformaldehyde) fixed A549 cells using anti-Vitronectin/S-Protein Monoclonal Antibody at dilution of 1:50.
Immunofluorescent analysis of (4% Paraformaldehyde) fixed HepG2 cells using anti-Vitronectin/S-Protein Monoclonal Antibody at dilution of 1:50.
Flow cytometric analysis of human Vitronectin/S-Protein expression on HepG2 cells. Cells were stained with purified anti-Human Vitronectin/S-Protein, then a Alexa Fluor 488-conjugated second step antibody. The histogram were derived from events with the forward and side light-scatter characteristics of intact cells.