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.
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
IP | Flow Cyt (Intra) | ICC/IF | IHC-P | WB | |
---|---|---|---|---|---|
Human | Tested | Tested | Tested | Tested | Tested |
Mouse | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Rat | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info - | Notes - |
Select an associated product type
Isoform 1Cleaves beta-linked terminal galactosyl residues from gangliosides, glycoproteins, and glycosaminoglycans.Isoform 2Has no beta-galactosidase catalytic activity, but plays functional roles in the formation of extracellular elastic fibers (elastogenesis) and in the development of connective tissue. Seems to be identical to the elastin-binding protein (EBP), a major component of the non-integrin cell surface receptor expressed on fibroblasts, smooth muscle cells, chondroblasts, leukocytes, and certain cancer cell types. In elastin producing cells, associates with tropoelastin intracellularly and functions as a recycling molecular chaperone which facilitates the secretions of tropoelastin and its assembly into elastic fibers.
Beta-galactosidase, Acid beta-galactosidase, Elastin receptor 1, Lactase, GLB1, ELNR1
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.
Beta-galactosidase, Acid beta-galactosidase, Elastin receptor 1, Lactase, GLB1, ELNR1
IgG
Rabbit
pH: 7.2 - 7.4
Constituents: 100% PBS
Liquid
Monoclonal
Yes
EPR26120-76
Affinity purification Protein A
Blue Ice
+4°C
Do Not Freeze
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
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.
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.
GLB1 also known as beta-galactosidase is an enzyme that catalyzes the hydrolysis of beta-galactosides into monosaccharides. The protein has a molecular mass of approximately 76 kDa. Researchers observe this enzyme expression in the lysosome where it functions to break down complex carbohydrates. Its activity depends on proper glycosylation and correct folding usually occurring within specific cellular compartments.
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.
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.
GLB1 mutations associate with conditions like GM1 gangliosidosis and Morquio syndrome type B. These are lysosomal storage disorders resulting from the accumulation of unmetabolized substrates. In these diseases hexosaminidase and other lysosomal enzymes show relationships with GLB1 illuminating complex interactions within cellular pathology. Therapeutic research aims to correct or enhance enzyme function seeking to alleviate disorder symptoms.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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] (Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174) 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
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Observed band size: 66 kDa
Exposure time: 15s
Blocking and diluting buffer and concentration: 5% NFDM/TBST Low expression: Daudi
Exposure time: 15 seconds
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174 at 1/500 (1.088 ug/ml) dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed 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: DaudiImage was taken with a confocal microscope(Leica-Microsystems, TCS SP8). Alexa Fluor® 594 Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker 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 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor? 488) preadsorbed at 1/1000 (2 ug/ml) dilution.
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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] (Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174) 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
All lanes: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/5000 dilution
Observed band size: 66 kDa
Exposure time: 15s
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (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: abAB305174 IP in SK-BR-3 whole cell lysate
Lane 3:Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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] (Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174) 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
Lane 3: Immunoprecipitation - Rabbit IgG, monoclonal [EPR25A] - Isotype Control (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730)
All lanes: Immunoprecipitation - VeriBlot for IP Detection Reagent (HRP) (VeriBlot for IP Detection Reagent (HRP) ab131366) at 1/5000 dilution
Observed band size: 66 kDa
Exposure time: 15s
GLB1/Beta-galactosidase was immunoprecipitated from 0.35 mg SK-BR-3 (human breast adenocarcinoma epithelial cell) whole cell lysate 10 ug with Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(VeriBlot for IP Detection Reagent (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: abAB305174 IP in SK-BR-3 whole cell lysate
Lane 3:Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) instead of Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174 in SK-BR-3 whole cell lysate
Blocking and dilution buffer and concentration: 5% NFDM/TBST.
Exposure time: 15 seconds
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174 at 1/500 dilution (0.1ug) (Red) (Red) compared with a Rabbit monoclonal IgG (Rabbit IgG, monoclonal [EPR25A] - Isotype Control 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, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 1/2000 dilution was used as the secondary antibody. Low expression control: Daudi.
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling GLB1/Beta-galactosidase with Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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.
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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.
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human prostate hyper tissue labeling GLB1/Beta-galactosidase with Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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.
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human placenta tissue labeling GLB1/Beta-galactosidase with Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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.
This data was developed using Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] ab305174, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human breast carcinoma tissue labeling GLB1/Beta-galactosidase with Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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 Anti-GLB1/Beta-galactosidase antibody [EPR26120-76] 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
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