Anti-GCH1 antibody [EPR27331-30] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal GCH1 antibody. Carrier free. Suitable for IP, IHC-P, WB and reacts with Mouse, Rat, Human samples.
View Alternative Names
DYT5, GCH, GCH1, GTP cyclohydrolase 1, GTP cyclohydrolase I, GTP-CH-I
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human colon tissue labeling GCH1 with ab307507 at 1/500 (1.044 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Positive staining on scattered cells in human colon (PMID : 22753274).The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human skeletal muscl tissue labeling GCH1 with ab307507 at 1/500 (1.044 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Negative control : No staining on human skeletal muscle.The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Human pancreas tissue labeling GCH1 with ab307507 at 1/500 (1.044 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Positive staining on human pancreatic islets.The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat colon tissue labeling GCH1 with ab307507 at 1/1000 (0.522 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Positive staining on scattered cells in rat colon.The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling GCH1 with ab307507 at 1/1000 (0.522 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Negative control : No staining on rat skeletal muscle.The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscl tissue labeling GCH1 with ab307507 at 1/1000 (0.522 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Negative control : No staining on mouse skeletal muscle.The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Rat pancreas tissue labeling GCH1 with ab307507 at 1/1000 (0.522 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Positive staining on rat pancreatic islets.The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse midbrain tissue labeling GCH1 with ab307507 at 1/1000 (0.522 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Positive staining on neurons of mouse midbrain (PMID : 10907721). The section was incubated with ab307507 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) was used. 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-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. Immunohistochemical analysis of paraffin-embedded Mouse stomach tissue labeling GCH1 with ab307507 at 1/1000 (0.522 ug/ml) followed by a ready to use LeicaDS9800 (Bond? Polymer Refine Detection) was used. Positive staining on scattered cells in mouse stomach.The section was incubated with ab307507 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) was used. Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IP
Supplier Data
Immunoprecipitation - Anti-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using ab307507, the same antibody clone in a different buffer formulation. GCH1 was immunoprecipitated from 0.35 mg Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate 10 ug with ab307507 at 1/30 dilution (2ug in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab307507 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution. Lane 1 : Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate 10 ug Lane 2 : ab307507 IP in Neuro-2a whole cell lysate Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab307507 in Neuro-2a whole cell lysate Blocking and dilution buffer and concentration : 5% NFDM/TBST. Exposure time : 6 seconds
All lanes:
Immunoprecipitation - Anti-GCH1 antibody [EPR27331-30] (<a href='/en-us/products/primary-antibodies/gch1-antibody-epr27331-30-ab307507'>ab307507</a>) at 1/1000 dilution
Lane 1:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate 10 μg
Lane 2:
Neuro-2a whole cell lysate
Lane 3:
Rabbit monoclonal IgG (<a href='/en-us/products/primary-antibodies/rabbit-igg-monoclonal-epr25a-isotype-control-ab172730'>ab172730</a>) instead of <a href='/en-us/products/primary-antibodies/gch1-antibody-epr27331-30-ab307507'>ab307507</a> in Neuro-2a 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: 27 kDa
false
Exposure time: 6s
- WB
Supplier Data
Western blot - Anti-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using 307507, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Negative control : K562 (PMID : 32778843) Exposure time :
All lanes:
Western blot - Anti-GCH1 antibody [EPR27331-30] (<a href='/en-us/products/primary-antibodies/gch1-antibody-epr27331-30-ab307507'>ab307507</a>) at 1/1000 dilution
Lane 1:
SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate 20 μg
Lane 2:
K562 (human chronic myelogenous leukemia lymphoblast) whole cell lysate 20 μg
Lane 3:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate 20 μg
Lane 4:
N9 (mouse microglia) whole cell lysate 20 μg
Lane 5:
PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate 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 1/100000 dilution
Observed band size: 27 kDa
false
Exposure time: 37s
- WB
Supplier Data
Western blot - Anti-GCH1 antibody [EPR27331-30] - BSA and Azide free (AB307508)
This data was developed using 307507, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : Negative control : skeletal muscle (PMID : 22798524) 180 seconds Exposure time :
All lanes:
Western blot - Anti-GCH1 antibody [EPR27331-30] (<a href='/en-us/products/primary-antibodies/gch1-antibody-epr27331-30-ab307507'>ab307507</a>) at 1/1000 dilution
Lane 1:
Mouse liver tissue lysate 20 μg
Lane 2:
Mouse hypothalamus tissue lysate 20 μg
Lane 3:
Mouse skeletal muscle tissue lysate 20 μg
Lane 4:
Rat liver tissue lysate 20 μg
Lane 5:
Rat hypothalamus tissue lysate 20 μg
Lane 6:
Rat skeletal muscle tissue lysate 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 1/100000 dilution
Observed band size: 27 kDa
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-GCH1 antibody [EPR27331-30]
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
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'.
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