Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal GLB1/Beta-galactosidase antibody. Carrier free. Suitable for IP, Flow Cyt (Intra), ICC/IF, IHC-P, WB and reacts with Human samples.
View Alternative Names
ELNR1, GLB1, Beta-galactosidase, Acid beta-galactosidase, Elastin receptor 1, Lactase
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human breast carcinoma tissue labeling GLB1/Beta-galactosidase with ab305174 at 1/500 dilution (1.088 ug/ml) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The immunostaining was performed on a Leica Biosystems BOND® RX instrument counterstained with Hematoxylin. Positive staining on human breast carcinoma. The section was incubated with ab305174 for 30 mins at room temperature. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human prostate hyper tissue labeling GLB1/Beta-galactosidase with ab305174 at 1/500 (1.088 ug/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining on human prostate hyperplasia (PMID : 25876105, 28234906).The section was incubated with ab305174 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 100% Methanol permeabilized SK-BR-3 (human breast adenocarcinoma epithelial cell) cells labeling GLB1/Beta-galactosidase with ab305174 at 1/500 (1.088 ug/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 (2 ug/ml) dilution (Green). Confocal image showing cytoplasmic punctate staining in SK-BR-3 cell line. Low expression : Daudi. Image was taken with a confocal microscope(Leica-Microsystems, TCS SP8). ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 ug/ml) dilution (Red). The nuclear counterstain was DAPI (Blue). Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded (A) MCF-7 (human bre tissue labeling GLB1/Beta-galactosidase with ab305174 at 1/500 (1.088 ug/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining on (A) MCF-7 cell pellet and (B) SK-BR-3 cell pellet; almost no staining on (C) Daudi cell pellet. The section was incubated with ab305174 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human placenta tissue labeling GLB1/Beta-galactosidase with ab305174 at 1/500 (1.088 ug/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining on human placenta (PMID : 8383699).The section was incubated with ab305174 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling GLB1/Beta-galactosidase with ab305174 at 1/500 (1.088 ug/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining on human liver. The section was incubated with ab305174 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin. Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Daudi (human Burkitt's lymphoma lymphoblast, Left) / SK-BR-3 (human breast adenocarcinoma epithelial cell, Right) cells labelling GLB1/Beta-galactosidase with ab305174 at 1/500 dilution (0.1ug) (Red) (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/2000 dilution was used as the secondary antibody. Low expression control : Daudi.
- IP
Supplier Data
Immunoprecipitation - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation.
GLB1/Beta-galactosidase was immunoprecipitated from 0.35 mg SK-BR-3 (human breast adenocarcinoma epithelial cell) whole cell lysate 10 ug with ab305174 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab305174 at 1/1000 dilution. VeriBlot for IP secondary antibody (HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : SK-BR-3 (human breast adenocarcinoma epithelial cell) whole cell lysate 10 ug
Lane 2 : ab305174 IP in SK-BR-3 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab305174 in SK-BR-3 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 15 seconds
All lanes:
Immunoprecipitation - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] (<a href='/en-us/products/primary-antibodies/glb1-beta-galactosidase-antibody-epr26120-76-ab305174'>ab305174</a>) at 1/1000 dilution
Lane 1:
SK-BR-3 (human breast adenocarcinoma epithelial cell) whole cell lysate 10 μg
Lane 2:
SK-BR-3 whole cell lysate
Secondary
All lanes:
Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/5000 dilution
Observed band size: 66 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Exposure time :
All lanes:
Western blot - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] (<a href='/en-us/products/primary-antibodies/glb1-beta-galactosidase-antibody-epr26120-76-ab305174'>ab305174</a>) at 1/1000 dilution
Lane 1:
Human lu tissue lysate 20 μg
Lane 2:
Human clolon tissue lysate 20 μg
Lane 3:
Human liver tissue lysate 20 μg
Lane 4:
Human testis tissue lysate 10 μg
Lane 5:
Human placenta tissue lysate 10 μg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/5000 dilution
Observed band size: 66 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] - BSA and Azide free (AB305175)
This data was developed using ab305174, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Low expression : Daudi 15 seconds Exposure time :
All lanes:
Western blot - Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] (<a href='/en-us/products/primary-antibodies/glb1-beta-galactosidase-antibody-epr26120-76-ab305174'>ab305174</a>) at 1/1000 dilution
Lane 1:
MCF7 (human breast adenocarcinoma epithelial cell), whole cell lysate 10 μg
Lane 2:
SK-BR-3 (human breast adenocarcinoma epithelial cell), whole cell lysate 10 μg
Lane 3:
Daudi (human Burkitts lymphoma lymphoblast), whole cell lysate 10 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 1/100000 dilution
Observed band size: 66 kDa
false
Exposure time: 15s
Related conjugates and formulations (2)
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Anti-GLB1/Beta-galactosidase antibody [EPR26120-76]
-
665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76]
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
GLB1 is integral to the degradation and recycling of glycoproteins and glycolipids in the cell. It forms part of the lysosomal enzyme complex responsible for processing macromolecules. Without its function the accumulation of substrates can occur affecting cellular metabolism. The enzyme ensures that metabolic waste is efficiently processed linking GLB1 to cellular homeostasis.
Pathways
Beta-galactosidase participates in the lysosomal storage and glycan metabolism pathways. It is important for the catabolism of glycoside forms of hormones and other biologically-active molecules. In these pathways GLB1 interacts with proteins such as hexosaminidase creating a network of lysosomal enzymes. These interactions enable coordinated degradation of glycoproteins maintaining balance within cellular systems.
Product protocols
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Target data
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