Anti-Chromogranin A antibody [RM1025] - BSA and Azide free
- RabMAb
- Recombinant
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(1 Publication)
Rabbit Recombinant Multiclonal Chromogranin A antibody. Carrier free. Suitable for IHC-P, ICC/IF, IP, Flow Cyt (Intra), ELISA, WB, IHC-Fr and reacts with Mouse, Rat, Human samples. Cited in 1 publication.
View Alternative Names
Chromogranin-A, CgA, Pituitary secretory protein I, SP-I, CHGA
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Jurkat (Human T cell leukemia T lymphocyte / Left) and SH-SY5Y (Human neuroblastoma epithelial cell / Right) cells labelling Chromogranin A with ab283265 at 1/500 dilution (0.1 μg) compared with an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue). A Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/2000 dilution was used as the secondary antibody.
Negative control : Jurkat.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human stomach tissue labelling Chromogranin A with ab283265 at 1/5000 dilution (0.107 μg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Positive staining on the endocrine cells in human stomach. The section was incubated with ab283265 overnight at 4℃. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human pancreas tissue labelling Chromogranin A with ab283265 at 1/5000 dilution (0.107 μg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Positive staining on the islet in human pancreas. The section was incubated with ab283265 overnight at 4℃. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0)
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized SH-SY5Y (human neuroblastoma cell line from bone marrow) cells labelling Chromogranin A with ab283265 at 1/50 dilution (10.74 μg/ml), followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 μg/ml) (Green). Confocal image showing cytoplasmic staining in subsets of SH-SY5Y cells.
Negative control : Jurkat.
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 μg/ml) (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.
- IP
Supplier Data
Immunoprecipitation - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Chromogranin A was immunoprecipitated from 0.35 mg SH-SY5Y (Human neuroblastoma epithelial cell) whole cell lysate with ab283265 at 1/30 dilution (2 μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab283265 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP)(ab131366) was used at 1/5000 dilution.
Lane 1 : SH-SY5Y (Human neuroblastoma epithelial cell) whole cell lysate 10ug
Lane 2 : ab283265 IP in SH-SY5Y whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab283265 in SH-SY5Y whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 30 seconds
Lower bands could be cleavage fragment. (PMID : 17991725)
All lanes:
Immunoprecipitation - Anti-Chromogranin A antibody [RM1025] (<a href='/en-us/products/primary-antibodies/chromogranin-a-antibody-rm1025-ab283265'>ab283265</a>)
Predicted band size: 50 kDa
Observed band size: 75 kDa
false
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse colon (fresh) tissue labeling Chromogranin A with ab283265 at 1/500 dilution (1.074 μg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 μg/ml) (Green). Positive satining on mouse colon is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat adrenal gland tissue labelling Chromogranin A with ab283265 at 1/5000 dilution (0.107 μg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Positive staining in the rat adrenal gland. The section was incubated with ab283265 overnight at 4℃. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat pancreas tissue labelling Chromogranin A with ab283265 at 1/5000 dilution (0.107 μg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Positive staining on the islet in rat pancreas. The section was incubated with ab283265 overnight at 4℃. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse pancreas tissue labelling Chromogranin A with ab283265 at 1/5000 dilution (0.107 μg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Positive staining on the islet in mouse pancreas. The section was incubated with ab283265 overnight at 4℃. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0)
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat colon (fresh) tissue labeling Chromogranin A with ab283265 at 1/500 dilution (1.074 μg/ml) followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (2 μg/ml) (Green). Positive staining on rat colon is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed.
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized Neuro-2a (mouse neuroblastoma cell line) cells labelling Chromogranin A with ab283265 at 1/50 dilution (10.74 μg/ml), followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (2 μg/ml) (Green). Confocal image showing cytoplasmic staining in of Neuro-2a cells.
Negative control : NIH/3T3 (PMID : 7615829).
ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) was used to counterstain tubulin at 1/200 dilution (2.5 μg/ml) (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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse adrenal gland tissue labelling Chromogranin A with ab283265 at 1/5000 dilution (0.107 μg/ml) followed by a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer). Positive staining in the mouse adrenal gland. The section was incubated with ab283265 overnight at 4℃. Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use Goat Anti-Rabbit IgG H&L (HRP polymer).
Heat mediated antigen retrieval using ab93678 (citrate buffer, pH 6.0)
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized NIH/3T3 (Mouse embryonic fibroblast / Left) and Neuro-2a (Mouse neuroblastoma neuroblast / Right) cells labelling Chromogranin A with ab283265 at 1/500 dilution (0.1 μg / 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, ab150077) at 1/2000 dilution was used as the secondary antibody.
Negative control : NIH/3T3. (PMID : 7615829)
- IP
Supplier Data
Immunoprecipitation - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Chromogranin A was immunoprecipitated from 0.35 mg Neuro-2a (Mouse neuroblastoma neuroblast) whole cell lysate with ab283265 at 1/30 dilution (2 μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab283265 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 10ug
Lane 2 : ab283265 IP in Neuro-2a whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab283265 in Neuro-2a whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 3 min
Lower bands could be cleavage fragment. (PMID : 17991725)
All lanes:
Immunoprecipitation - Anti-Chromogranin A antibody [RM1025] (<a href='/en-us/products/primary-antibodies/chromogranin-a-antibody-rm1025-ab283265'>ab283265</a>)
Predicted band size: 50 kDa
Observed band size: 75 kDa
false
- WB
Lab
Western blot - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Negative control : Jurkat.
The molecular weight observed is consistent with what has been described in the literature (PMID : 14734658, 21052719).
This blot was developed using a higher sensitivity ECL substrate.
Exposure time : 3 min
All lanes:
Western blot - Anti-Chromogranin A antibody [RM1025] (<a href='/en-us/products/primary-antibodies/chromogranin-a-antibody-rm1025-ab283265'>ab283265</a>) at 1/1000 dilution
Lane 1:
Human adrenal gland lysate at 20 µg
Lane 2:
SH-SY5Y (Human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
Jurkat (Human T cell leukemia T lymphocyte) whole cell lysate at 20 µg
Lane 4:
Neuro-2a (Mouse neuroblastoma neuroblast) whole cell lysate at 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
Predicted band size: 50 kDa
Observed band size: 20 kDa,75 kDa
false
- WB
Lab
Western blot - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
Negative control : NIH/3T3. (PMID : 7615829)
Exposure time : Lane 1-2 : 5 seconds Lane 3-5 : 92 seconds
All lanes:
Western blot - Anti-Chromogranin A antibody [RM1025] (<a href='/en-us/products/primary-antibodies/chromogranin-a-antibody-rm1025-ab283265'>ab283265</a>) at 1/1000 dilution
Lane 1:
Mouse adrenal gland lysate at 20 µg
Lane 2:
Rat adrenal gland lysate at 20 µg
Lane 3:
Neuro-2a (Mouse neuroblastoma neuroblast) whole cell lysate at 20 µg
Lane 4:
NIH/3T3 (Mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 5:
PC-12 (Rat adrenal gland pheochromocytoma) whole cell lysate at 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
Predicted band size: 50 kDa
Observed band size: 20 kDa,75 kDa
false
- ELISA
Supplier Data
ELISA - Anti-Chromogranin A antibody [RM1025] - BSA and Azide free (AB283286)
This data was developed using ab283265, the same antibody clone in a different buffer formulation.
ELISA using ab283265 at varying antibody concentrations and antigen concentration at 1000 ng/ml. An Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) (1/2500) was used as the secondary antibody.
Related conjugates and formulations (1)
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Anti-Chromogranin A antibody [RM1025]
Reactivity data
Product details
ab283286 is the carrier-free version of ab283265.
What are recombinant multiclonals?
Recombinant multiclonals are a mixture of recombinant antibodies co-expressed from a library of heavy and light chains. They offer several advantages including:
- - The sensitivity of polyclonal antibodies by recognising multiple epitopes
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
View our range of recombinant multiclonal antibodies.
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.
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
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
Chromogranin A assists in the regulation of secretory pathways across multiple neuroendocrine systems. It plays a role in hormone storage conversion to active peptides and regulates the exocytosis of hormones. CgA acts within a complex contributing to secretory granule biogenesis and influencing intravesicular acidity. As a regulatory component the exact physiological roles are diverse impacting cardiovascular metabolic and immunological processes.
Pathways
Chromogranin A is involved in pathways such as the catecholamine synthesis and release pathway and the serotonergic pathway. Within these pathways it interacts with proteins like secretogranin II and parathyroid hormone (PTH). These interactions modulate neurotransmitter storage and secretion across various systems. CgA's bioactive peptides also contribute to modulating physiological processes like vasoconstriction and insulin regulation linking it closely with these signaling cascades.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Biomedical reports 19:102 PubMed38025835
2023
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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