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Read our guarantee »Products:Neuroscience >> Cell Type Marker >> Neural Stem Cell marker
Anti-HMGA2 antibody
See all HMGA2 products (5) ...
Rabbit polyclonal to HMGA2
ICC/IF, IP, WBmore details
Reacts with
Mouse, Human
Synthetic peptide corresponding to C-terminal region of human HMGA2. The amino acid sequence is unavailable.
SW579 cells. Colon carcinoma.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.1% Sodium Azide
Constituents: 1% BSA, 10mM PBS, pH 7.4
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgG
Developmental Biology >> Post embryonic development >> Aging
Cancer >> Cell cycle >> Cell differentiation
Stem Cells >> Neural Stem Cells >> Intracellular
Epigenetics and Nuclear Signaling >> Cell cycle >> Cell Differentiation
Neuroscience >> Neurology process >> Neurogenesis
Neuroscience >> Neurology process >> Metabolism
Epigenetics and Nuclear Signaling >> Histones >> HMGs
Neuroscience >> Cell Type Marker >> Neural Stem Cell marker
Our Abpromise guarantee covers the use of ab41878 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 5 µg/ml
IP: Use at an assay dependent concentration.
WB: Use a concentration of 2 - 4 µg/ml.Detects a band of approximately 17 kDa (predicted molecular weight: 12 kDa).
Functions as a transcriptional regulator. Functions in cell cycle regulation through CCNA2.
Note=A chromosomal aberration involving HMGA2 is associated with a subclass of benign mesenchymal tumors known as lipomas. Translocation t(3;12)(q27-q28;q13-q15) with LPP is shown in lipomas. HMGA2 is also fused with a number of other genes in lipomas.
Note=A chromosomal aberration involving HMGA2 is associated with pulmonary chondroid hamartomas. Translocation t(3;12)(q27-q28;q14-q15) with LPP is detected in pulmonary chondroid hamartomas.
Note=A chromosomal aberration involving HMGA2 is associated with parosteal lipomas. Translocation t(3;12)(q28;q14) with LPP is also shown in one parosteal lipoma.
Note=A chromosomal aberration involving HMGA2 is found in uterine leiomyoma. Translocation t(12;14)(q15;q23-24) with RAD51L1. Chromosomal rearrangements involving HMGA2 do not seem to be the principle pathobiological mechanism in uterine leiomyoma.
Belongs to the HMGA family.
Contains 3 A.T hook DNA-binding domains.
Expressed predominantly during embryogenesis.
Regulated by cell cycle-dependent phosphorylation which alters its DNA binding affinity.
Nucleus.
Target information above from: UniProt accessionP52926
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry/ Immunofluorescence - Anti-HMGA2 antibody (ab41878)

ICC/IF image of ab41878 stained HepG2 cells. The cells were 100% methanol fixed (5 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 (ab41878, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit 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.
Western blot - HMGA2 antibody (ab41878)

Anti-HMGA2 antibody (ab41878) at 1 µg/ml + MOLT4 (Human acute lymphoblastic leukemia cell line) Whole Cell Lysate at 10 µg
Secondary
Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP), pre-adsorbed (ab97080) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 12 kDa
Observed band size : 17 kDa (why is the actual band size different from the predicted?)
Additional bands at : 42 kDa,74 kDa. We are unsure as to the identity of these extra bands.
Exposure time : 20 minutes
HMGA2 contains a number of potential phosphorylation sites (SwissProt) which may explain its migration at a higher molecular weight than predicted.
Immunoprecipitation - Anti-HMGA2 antibody (ab41878)

HMGA2 was immunoprecipitated using 0.5mg HepG2 whole cell extract, 5ug of Rabbit polyclonal to HMGA2and 50µl of protein G magnetic beads (lane 1). The antibody was incubated with the Protein G beads for 10min under agitation. No antibody was added to the control (lane 2). HepG2 whole cell extractdiluted in RIPA buffer was added to each sample and incubated for 10min under agitation. Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab41878. Secondary: Clean blot (HRP conjugate) at 1/1000 dilution. Bands: 17kDa; HMGA2: 55kDa; Heavy Chains: Non Specific - 45 and 130kDa: We are unsure as to the identity of this extra band.
This product has been referenced in:
See all 3 publications for this product
Publishing research using ab41878? Please let us know so that we can cite the reference in this datasheet
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ICC/IF image of ab41878 stained HepG2 cells. The cells were 100% methanol fixed (5 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 (ab41878, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit 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.

Anti-HMGA2 antibody (ab41878) at 1 µg/ml + MOLT4 (Human acute lymphoblastic leukemia cell line) Whole Cell Lysate at 10 µg
Secondary
Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (HRP), pre-adsorbed (ab97080) at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 12 kDa
Observed band size : 17 kDa (why is the actual band size different from the predicted?)
Additional bands at : 42 kDa,74 kDa. We are unsure as to the identity of these extra bands.
Exposure time : 20 minutes
HMGA2 contains a number of potential phosphorylation sites (SwissProt) which may explain its migration at a higher molecular weight than predicted.

HMGA2 was immunoprecipitated using 0.5mg HepG2 whole cell extract, 5ug of Rabbit polyclonal to HMGA2and 50µl of protein G magnetic beads (lane 1). The antibody was incubated with the Protein G beads for 10min under agitation. No antibody was added to the control (lane 2). HepG2 whole cell extractdiluted in RIPA buffer was added to each sample and incubated for 10min under agitation. Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab41878. Secondary: Clean blot (HRP conjugate) at 1/1000 dilution. Bands: 17kDa; HMGA2: 55kDa; Heavy Chains: Non Specific - 45 and 130kDa: We are unsure as to the identity of this extra band.
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