Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal NAGLU/NAG antibody. Carrier free. Suitable for ICC/IF, WB, Flow Cyt (Intra), IHC-P and reacts with Mouse, Human, Rat samples.
View Alternative Names
UFHSD1, NAGLU, Alpha-N-acetylglucosaminidase, N-acetyl-alpha-glucosaminidase, NAG
- WB
Supplier Data
Western blot - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure times : Lanes 1-2, 5-6 : 3 minutes; Lanes 3-4 : 30 seconds.
Lanes 1 - 4:
Western blot - Anti-NAGLU/NAG antibody [EPR20708] (<a href='/en-us/products/primary-antibodies/naglu-nag-antibody-epr20708-ab214671'>ab214671</a>) at 1/2000 dilution
Lanes 5 - 6:
Western blot - Anti-NAGLU/NAG antibody [EPR20708] (<a href='/en-us/products/primary-antibodies/naglu-nag-antibody-epr20708-ab214671'>ab214671</a>) at 1/1000 dilution
Lane 1:
Mouse colon lysate at 20 µg
Lane 2:
Rat testis lysate at 20 µg
Lane 3:
Mouse testis lysate at 20 µg
Lane 4:
Rat colon lysate at 20 µg
Lane 5:
Rat liver lysate at 10 µg
Lane 6:
Rat spleen lysate at 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
Predicted band size: 82 kDa
Observed band size: 82 kDa
true
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human liver tissue labeling NAGLU/NAG with ab214671 at 1/4000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Granular cytoplasmic staining on human liver (PMID : 4291567, PMID : 8776591). Counter stained with hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed HepG2 (human liver hepatocellular carcinoma cell line) cell line labeling NAGLU/NAG with ab214671at 1/50 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat kidney tissue labeling NAGLU/NAG with ab214671 at 1/4000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Granular cytoplasmic staining on rat kidney tubules (PMID : 4291567, PMID : 24244710). Counter stained with hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- Flow Cyt (Intra)
Unknown
Flow Cytometry (Intracellular) - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Intracellular flow cytometric analysis of 4% paraformaldehyde-fixed Hepa1-6 (mouse hepatoma epithelial cell line) cell line labeling NAGLU/NAG with ab214671at 1/50 dilution (red) compared with a Rabbit IgG, monoclonal [EPR25A] - Isotype Control (ab172730) (black) and an unlabeled control (cells without incubation with primary antibody and secondary antibody) (blue). Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/2000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human kidney tissue labeling NAGLU/NAG with ab214671 at 1/4000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Granular cytoplasmic staining on human kidney tubules (PMID : 4291567, PMID : 24244710). Counter stained with hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed HepG2 (human liver hepatocellular carcinoma cell line) cells labeling NAGLU/NAG with ab214671 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on HepG2 cell line.
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse kidney tissue labeling NAGLU/NAG with ab214671 at 1/4000 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) Ready to use. Granular cytoplasmic staining on mouse kidney tubules (PMID : 4291567, PMID : 24244710). Counter stained with hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) Ready to use.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed Hepa1-6 (mouse hepatoma epithelial cell line) cells labeling NAGLU/NAG with ab214671 at 1/100 dilution followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution (green). Confocal image showing cytoplasmic staining on Hepa1-6 cell line.
The nuclear counter stain is DAPI (blue). Tubulin is detected with Anti-alpha Tubulin antibody [DM1A] - Microtubule Marker (Alexa Fluor® 594) (ab195889) (red) at 1/200 dilution.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody at 1/1000 dilution.
- WB
Supplier Data
Western blot - Anti-NAGLU/NAG antibody [EPR20708] - BSA and Azide free (AB251547)
This data was developed using ab214671, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
Exposure times : Lanes 1-2 : 1 minute; Lanes 3-4 : 30 seconds.
Lanes 1 - 3:
Western blot - Anti-NAGLU/NAG antibody [EPR20708] (<a href='/en-us/products/primary-antibodies/naglu-nag-antibody-epr20708-ab214671'>ab214671</a>) at 1/1000 dilution
Lane 4:
Western blot - Anti-NAGLU/NAG antibody [EPR20708] (<a href='/en-us/products/primary-antibodies/naglu-nag-antibody-epr20708-ab214671'>ab214671</a>) at 1/5000 dilution
Lane 1:
Human placenta lysate at 20 µg
Lane 2:
Human liver lysate at 20 µg
Lane 3:
Human fetal kidney lysate at 10 µg
Lane 4:
HepG2 (human liver hepatocellular carcinoma cell line) whole cell lysate at 10 µg
Secondary
Lanes 1 - 2:
Western blot - VeriBlot for IP Detection Reagent (HRP) (<a href='/en-us/products/reagents/veriblot-for-ip-detection-reagent-hrp-ab131366'>ab131366</a>) at 1/4000 dilution
Lanes 3 - 4:
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
Predicted band size: 82 kDa
Observed band size: 82 kDa
true
Related conjugates and formulations (10)
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Anti-NAGLU/NAG antibody [EPR20708]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-NAGLU/NAG antibody [EPR20708]
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578 PE
PE Anti-NAGLU/NAG antibody [EPR20708]
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HRP Anti-NAGLU/NAG antibody [EPR20708]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-NAGLU antibody [EPR20708]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-NAGLU antibody [EPR20708]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-NAGLU antibody [EPR20708]
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-NAGLU/NAG antibody [EPR20708]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-NAGLU antibody [EPR20708]
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660 APC
APC Anti-NAGLU/NAG antibody [EPR20708]
Reactivity data
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Why is this recommended?
We recommend this product because it’s often used in the same experiment or related research.
We advise that you always check the datasheet to ensure it fits your experiments, or contact ourtechnical teamfor help.
Product details
ab251547 is the carrier-free version of ab214671.
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
NAGLU facilitates the degradation of heparan sulfate in conjunction with other enzymes as part of a degradation complex within the lysosome. NAGLU's action is essential for maintaining the balance of heparan sulfate levels inside cells which is important for cellular health and function. Without the proper function of this enzyme heparan sulfate accumulates within lysosomes due to incomplete catabolism leading to cellular dysfunction and related pathologies.
Pathways
NAGLU functions critically in the glycosaminoglycan degradation pathway. This pathway involves several enzymes including iduronate-2-sulfatase which acts upstream of NAGLU. Together they ensure the breakdown of complex sugars such as heparan sulfate. NAGLU also participates in the larger lysosomal degradation pathway collaborating with other lysosomal enzymes to ensure proper breakdown and recycling of cellular materials.
Product protocols
- Visit the General protocols
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Product promise
Associated Products
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