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Read our guarantee »Products:Signal Transduction >> Cytoskeleton / ECM >> Cell Adhesion >> Integrins >> Alpha
Anti-Integrin alpha 2+beta 1 antibody [16B4]
See all Integrin alpha 2+beta 1 products (3) ...
Mouse monoclonal [16B4] to Integrin alpha 2+beta 1
We have data to indicate that this antibody may not cross react with Rat. However, this has not been conclusively tested and expression levels may vary in certain cell lines/tissues.
ICC/IF, IHC-P, IP, WB, Flow Cyt, ELISA, IHC-Frmore details
Reacts with
Human
Purified human beta 1 preparation from HT1080 fibrosarcoma cell extract.
In IF, this antibody gave a positive signal in HepG2 cells.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: PBS, pH 7.4
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IgG fraction
ab30483 was purified from tissue culture supernatant
ab30483 is identified as capable of immunoprecipitating a non-reducible alpha subunit from I125 surface labelled Human cell line extract. It is confirmed as specific to the alpha 2 subunit by relative expression of antigen on various cell lines by FACS, and its recognition of affinity purified alpha 2 beta 1 in dot blots.
Monoclonal
16B4
x63-Ag8.653
IgG1
Cancer >> Cancer Metabolism >> Response to hypoxia
Signal Transduction >> Cytoskeleton / ECM >> Cell Adhesion >> Integrins >> Beta
Signal Transduction >> Cytoskeleton / ECM >> Cell Adhesion >> Integrins >> Alpha
Our Abpromise guarantee covers the use of ab30483 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use a concentration of 1 µg/ml
IHC-P: Use at an assay dependent dilution. Perform heat mediated antigen retrieval before commencing with IHC staining protocol.(Tris/EDTA pH 9.0 is recommended for this purpose.)
IP: Use a concentration of 25 - 50 µg/ml.
WB: Use at an assay dependent dilution. Predicted molecular weight: 131 kDa.
Flow Cyt: Use a concentration of 30 µg/ml
ELISA: Use a concentration of 10 µg/ml
IHC-Fr: Use a concentration of 30 - 40 µg/ml.
Integrins are heterodimeric proteins made up of alpha and beta subunits. At least 18 alpha and 8 beta subunits have been described in mammals. Integrin family members are membrane receptors involved in cell adhesion and recognition in a variety of processes including embryogenesis, hemostasis, tissue repair, immune response and metatastatic diffusion of tumour cells.
Cell Membrane; single-pass type I membrane protein
Immunocytochemistry/ Immunofluorescence - Integrin alpha 2+beta 1 antibody [16B4] (ab30483)
![Immunocytochemistry/ Immunofluorescence - Integrin alpha 2+beta 1 antibody [16B4] (ab30483)](/ps/datasheet/images/30/ab30483/Integrin-alpha-2beta-1-Primary-antibodies-ab30483-2.jpg)
ICC/IF image of ab30483 stained HepG2 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab30483, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM. This antibody also gave a positive result in 4% PFA fixed (10 min) MCF7 cells at 1µg/ml.
Immunocytochemistry/ Immunofluorescence - Integrin alpha 2+beta 1 antibody [16B4] (ab30483)
![Immunocytochemistry/ Immunofluorescence - Integrin alpha 2+beta 1 antibody [16B4] (ab30483)](/ps/datasheet/Images/30/ab30483/ab30483_1.jpg)
ab30483 staining human breast cancer cells by ICC/IF. Cells were PFA fixed and blocked with 1% serum for 16 hours at 20°C prior to incubating with ab30483 (at 30µg/ml) for 16 hours at 4°C. An Alexa Fluor® 488 conjugated goat anti-mouse antibody, diluted 1/200, was used as the secondary.
This image is courtesy of an Abreview submitted by Dr Sharon Sneddon
This product has been referenced in:
See all 3 publications for this product
Publishing research using ab30483? Please let us know so that we can cite the reference in this datasheet
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![Immunocytochemistry/ Immunofluorescence - Integrin alpha 2+beta 1 antibody [16B4] (ab30483)](/ps/datasheet/images/30/ab30483/Integrin-alpha-2beta-1-Primary-antibodies-ab30483-2.jpg)
ICC/IF image of ab30483 stained HepG2 cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab30483, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM. This antibody also gave a positive result in 4% PFA fixed (10 min) MCF7 cells at 1µg/ml.
![Immunocytochemistry/ Immunofluorescence - Integrin alpha 2+beta 1 antibody [16B4] (ab30483)](/ps/datasheet/Images/30/ab30483/ab30483_1.jpg)
ab30483 staining human breast cancer cells by ICC/IF. Cells were PFA fixed and blocked with 1% serum for 16 hours at 20°C prior to incubating with ab30483 (at 30µg/ml) for 16 hours at 4°C. An Alexa Fluor® 488 conjugated goat anti-mouse antibody, diluted 1/200, was used as the secondary.
This image is courtesy of an Abreview submitted by Dr Sharon Sneddon
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