Anti-GNA13 antibody [EPR5436]
- RabMAb
- Recombinant
- KO Validated
- What is this?
4
(1 Review)
|
(22 Publications)
Rabbit Recombinant Monoclonal GNA13 antibody. Suitable for IHC-P, WB and reacts with Mouse, Rat, Human samples. Cited in 22 publications.
View Alternative Names
Guanine nucleotide-binding protein subunit alpha-13, G alpha-13, G-protein subunit alpha-13, GNA13
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GNA13 antibody [EPR5436] (AB128900)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human bladder carcinoma tissue sections labeling GNA13 with Purified ab128900 at 1 : 1000 dilution (1.2 μg/ml). Heat mediated antigen retrieval was performed using EDTA Buffer, pH9.0. Tissue was counterstained with Hematoxylin. ImmunoHistoProbe one step HRP Polymer (ready to use) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GNA13 antibody [EPR5436] (AB128900)
Unpurified ab128900, at a 1/250 dilution, staining GNA13 in paraffin embedded Human bladder carcinoma tissue by Immunohistochemistry.
Heat mediated antigen retrieval was performed with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GNA13 antibody [EPR5436] (AB128900)
Unpurified ab128900, at a 1/250 dilution, staining GNA13 in paraffin embedded Human kidney tissue by Immunohistochemistry.
Heat mediated antigen retrieval was performed with citrate buffer pH 6 before commencing with IHC staining protocol.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GNA13 antibody [EPR5436] (AB128900)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of rat stomach tissue sections labeling GNA13 with Purified ab128900 at 1 : 1000 dilution (1.2 μg/ml). Heat mediated antigen retrieval was performed using EDTA Buffer, pH9.0. Tissue was counterstained with Hematoxylin. ImmunoHistoProbe one step HRP Polymer (ready to use) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GNA13 antibody [EPR5436] (AB128900)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of mouse stomach tissue sections labeling GNA13 with Purified ab128900 at 1 : 1000 dilution (1.2 μg/ml). Heat mediated antigen retrieval was performed using EDTA Buffer, pH9.0. Tissue was counterstained with Hematoxylin. ImmunoHistoProbe one step HRP Polymer (ready to use) secondary antibody was used at 1 : 0 dilution. PBS instead of the primary antibody was used as the negative control.
- WB
Lab
Western blot - Anti-GNA13 antibody [EPR5436] (AB128900)
Lanes 1 - 2 : Merged signal (red and green). Green - ab128900 observed at 45 kDa. Red - loading control ab8245 (Mouse anti-GAPDH antibody [6C5]) observed at 37 kDa.
ab128900 was shown to react with GNA13 in wild-type HeLa cells in Western blot with loss of signal observed in GNA13 knockout cell line ab264846 (GNA13 knockout cell lysate ab257451). Wild-type HeLa and GNA13 knockout cell lysates were subjected to SDS-PAGE. Membranes were blocked in 3 % milk in TBS-T (0.1 % Tween®) before incubation with ab128900 and ab8245 (Mouse anti-GAPDH antibody [6C5]) overnight at 4 °C at a 1 in 1000 dilution and a 1 in 20000 dilution respectively. Blots were incubated with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed (ab216773) and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed (ab216776) secondary antibodies at 1 in 20000 dilution for 1 h at room temperature before imaging.
All lanes:
Western blot - Anti-GNA13 antibody [EPR5436] (ab128900) at 1/1000 dilution
Lane 1:
Wild-type HeLa cell lysate at 20 µg
Lane 2:
GNA13 knockout HeLa cell lysate at 20 µg
Lane 2:
Western blot - Human GNA13 knockout HeLa cell line (<a href='/en-us/products/cell-lines/human-gna13-knockout-hela-cell-line-ab264846'>ab264846</a>)
Predicted band size: 44 kDa
Observed band size: 45 kDa
false
- WB
Unknown
Western blot - Anti-GNA13 antibody [EPR5436] (AB128900)
All lanes:
Western blot - Anti-GNA13 antibody [EPR5436] (ab128900) at 1/1000 dilution
Lane 1:
Y79 cell lysate at 10 µg
Lane 2:
293T cell lysate at 10 µg
Lane 3:
HepG2 cell lysate at 10 µg
Secondary
All lanes:
Goat anti-Rabbit HRP at 1/2000 dilution
Predicted band size: 44 kDa
false
- WB
Lab
Western blot - Anti-GNA13 antibody [EPR5436] (AB128900)
Blocking and diluting buffer : 5% NFDM/TBST
All lanes:
Western blot - Anti-GNA13 antibody [EPR5436] (ab128900) at 1/5000 dilution
Lane 1:
HepG2 (Human hepatocellular carcinoma epithelial cell) whole cell lysates at 20 µg
Lane 2:
Mouse brain lysates at 20 µg
Lane 3:
Rat brain lysates at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 44 kDa
Observed band size: 44 kDa
false
- WB
Lab
Western blot - Anti-GNA13 antibody [EPR5436] (AB128900)
Blocking and dilution buffer : 5% NFDM/TBST.
All lanes:
Western blot - Anti-GNA13 antibody [EPR5436] (ab128900) at 1/5000 dilution
Lane 1:
Mouse brain tissue lysate at 20 µg
Lane 2:
Rat brain tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Predicted band size: 44 kDa
Observed band size: 44 kDa
false
Exposure time: 30s
- OI-RD Scanning
Unknown
OI-RD Scanning - Anti-GNA13 antibody [EPR5436] (AB128900)
We have systematically measured KD (the equilibrium dissociation constant between the antibody and its antigen), of more than 840 recombinant antibodies to assess not only their individual KD values but also to see the average affinity of antibody. Based on the comparison with published literature values for mouse monoclonal antibodies, Recombinant antibodies appear to be on average 1-2 order of magnitude higher affinity.
Related conjugates and formulations (1)
-
Anti-GNA13 antibody [EPR5436] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The role of G protein subunit GNA13 involves participating in critical cellular functions such as cytoskeletal reorganization cell migration and proliferation. It is an integral part of the G12/G13 subunits` complex which plays a role in controlling cell dynamics and morphology. Through these activities GNA13 contributes to the regulation of processes like embryonic development and tissue repair. Additionally it influences cell behavior through the RhoA pathway affecting actin cytoskeleton and cell shape changes.
Pathways
GNA13 interacts with a variety of important signaling systems. One primary pathway where GNA13 is active is the Rho signaling pathway where it activates RhoA leading to changes in the actin cytoskeleton. This pathway is necessary for cellular processes like adhesion and motility. Additionally GNA13 participates in the mitogen-activated protein kinase (MAPK) pathway influencing cellular proliferation. Through these pathways GNA13 is related to proteins such as RhoGEFs which act as guanine nucleotide exchange factors and MAPKs essential in transmitting mitogenic signals.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (22)
Recent publications for all applications. Explore the full list and refine your search
Nature communications 16:1751 PubMed39966435
2025
Applications
Unspecified application
Species
Unspecified reactive species
The Journal of biological chemistry 301:108136 PubMed39730062
2024
Applications
Unspecified application
Species
Unspecified reactive species
Cell 185:1974-1985.e12 PubMed35512704
2022
Applications
Unspecified application
Species
Unspecified reactive species
Nature communications 13:487 PubMed35078997
2022
Applications
Unspecified application
Species
Unspecified reactive species
Molecules (Basel, Switzerland) 26: PubMed34885790
2021
Applications
Unspecified application
Species
Unspecified reactive species
Science advances 7:eabj6895 PubMed34788088
2021
Applications
Unspecified application
Species
Unspecified reactive species
Aging 13:14940-14967 PubMed34031265
2021
Applications
Unspecified application
Species
Unspecified reactive species
PloS one 16:e0246363 PubMed33626068
2021
Applications
Unspecified application
Species
Unspecified reactive species
Cell death & disease 12:54 PubMed33423045
2021
Applications
Unspecified application
Species
Unspecified reactive species
Breast cancer research : BCR 22:105 PubMed33023655
2020
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com