Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Monoclonal SGTB/SGT2 antibody. Carrier free. Suitable for ICC/IF, IP, WB, IHC-P and reacts with Human, Mouse, Rat samples. Cited in 1 publication.
View Alternative Names
SGT2, SGTB, Small glutamine-rich tetratricopeptide repeat-containing protein beta, Beta-SGT, Small glutamine-rich protein with tetratricopeptide repeats 2
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized SH-SY5Y (Human neuroblastoma from bone marrow cells) cells labeling SGTB/SGT2 with ab202419 at 1/100 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing nuclear and weakly cytoplasmic staining on SH-SY5Y cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab202419 at 1/100 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) cells labeling SGTB/SGT2 with ab202419 at 1/100 dilution, followed by Goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) secondary antibody at 1/500 dilution (green). Confocal image showing nuclear and cytoplasmic staining on U-87 MG cell line. The nuclear counter stain is DAPI (blue). Tubulin is detected with ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution and ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution (red).
The negative controls are as follows :
-ve control 1 : ab202419 at 1/100 dilution followed by ab150120 (AlexaFluor®594 Goat anti-Mouse secondary) at 1/500 dilution.
-ve control 2 : ab7291 (anti-Tubulin mouse mAb) at 1/1000 dilution followed by ab150077 (Alexa Fluor®488 Goat Anti-Rabbit IgG H&L) at 1/500 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cerebral cortex tissue labeling SGTB/SGT2 with ab202419 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on Human cerebral cortex tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cerebral cortex tissue labeling SGTB/SGT2 with ab202419 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on rat cerebral cortex tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebral cortex tissue labeling SGTB/SGT2 with ab202419 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (HRP) (ab97051) secondary antibody at 1/500 dilution. Cytoplasmic and nuclear staining on mouse cerebral cortex tissue is observed. Counter stained with Hematoxylin.
Secondary antibody only control : Used PBS instead of primary antibody, secondary antibody is Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/500 dilution.
Perform heat mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol.
- IP
Supplier Data
Immunoprecipitation - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
SGTB/SGT2 was immunoprecipitated from 1mg of Mouse brain whole cell lysate with ab202419 at 1/40 dilution. Western blot was performed from the immunoprecipitate using ab202419 at 1/1000 dilution. Anti-Rabbit IgG (HRP), specific to the non-reduced form of IgG, was used as secondary antibody at 1/1500 dilution.
Lane 1 : Mouse brain whole cell lysate 10 μg (Input). Lane 2 : ab202419 IP in Mouse brain whole cell lysate. Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab202419 in Mouse brain whole cell lysate.
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 1 second.
All lanes:
Immunoprecipitation - Anti-SGTB/SGT2 antibody [EPR17183] (<a href='/en-us/products/primary-antibodies/sgtb-sgt2-antibody-epr17183-ab202419'>ab202419</a>)
Predicted band size: 33 kDa
false
- WB
Supplier Data
Western blot - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature, PMID : 12878599.
All lanes:
Western blot - Anti-SGTB/SGT2 antibody [EPR17183] (<a href='/en-us/products/primary-antibodies/sgtb-sgt2-antibody-epr17183-ab202419'>ab202419</a>) at 1/2000 dilution
All lanes:
Human fetal brain lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 33 kDa
Observed band size: 37 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature, PMID : 12878599.
All lanes:
Western blot - Anti-SGTB/SGT2 antibody [EPR17183] (<a href='/en-us/products/primary-antibodies/sgtb-sgt2-antibody-epr17183-ab202419'>ab202419</a>) at 1/2000 dilution
All lanes:
HepG2 (Human liver hepatocellular carcinoma) cell lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 33 kDa
Observed band size: 37 kDa
false
Exposure time: 3min
- WB
Supplier Data
Western blot - Anti-SGTB/SGT2 antibody [EPR17183] - BSA and Azide free (AB251369)
This data was developed using ab202419, the same antibody clone in a different buffer formulation.
Blocking and dilution buffer : 5% NFDM/TBST.
The expression profile observed is consistent with what has been described in the literature, PMID : 12878599.
All lanes:
Western blot - Anti-SGTB/SGT2 antibody [EPR17183] (<a href='/en-us/products/primary-antibodies/sgtb-sgt2-antibody-epr17183-ab202419'>ab202419</a>) at 1/2000 dilution
Lane 1:
Mouse brain lysate at 10 µg
Lane 2:
Rat brain lysate at 10 µg
Lane 3:
PC-12 (Rat adrenal gland pheochromocytoma) cell lysate at 10 µg
Lane 4:
NIH/3T3 (Mouse embyro fibroblast cells) cell lysate at 10 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated at 1/1000 dilution
Predicted band size: 33 kDa
Observed band size: 37 kDa
false
Exposure time: 3min
Related conjugates and formulations (1)
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Anti-SGTB/SGT2 antibody [EPR17183]
Reactivity data
Product details
ab251369 is the carrier-free version of ab202419.
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
The co-chaperone activity of SGT2 facilitates essential cellular functions through its interaction with molecular chaperones. This protein plays a significant role in the protein quality control system within the endoplasmic reticulum (ER). SGT2 contributes to the functionality of the ER-associated degradation (ERAD) pathway by recognizing misfolded proteins destined for degradation. Through this action it supports cellular homeostasis and prevents the aggregation of misfolded proteins.
Pathways
SGT2 engages actively in the ERAD and heat shock response pathways. Within these pathways it works closely with chaperones like HSP70 and HSP90 to maintain protein quality control and cellular stress responses. SGT2 regulates the degradation of misfolded proteins which is important in the ERAD pathway for maintaining proteostasis. By coordinating with other co-chaperones SGT2 ensures the transfer of substrates to the ubiquitin-proteasome system therefore facilitating their removal and preventing cellular dysfunction.
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Journal of nanobiotechnology 22:800 PubMed39731111
2024
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'.
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