Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal CDGSH iron sulfur domain-containing protein 2 homolog antibody. Carrier free. Suitable for WB, ICC/IF, IHC-P and reacts with Recombinant fragment - Human, Human, Mouse, Rat samples.
View Alternative Names
CDGSH2, ERIS, ZCD2, CDGSH iron-sulfur domain-containing protein 2, Endoplasmic reticulum intermembrane small protein, MitoNEET-related 1 protein, Nutrient-deprivation autophagy factor-1, Miner1, NAF-1, Cdgsh2, Noxp70, Zcd2, CDGSH iron-sulfur domain-containing protein 2, MitoNEET-related 1 protein, Nervous system overexpressed protein 70, Miner1
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized HEK-293 (human embryonic kidney epithelial cell) cells labelling CISD2 with ab325526 at 1/200 (2.495 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Confocal image showing cytoplasmic staining in HEK-293 cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-KDEL mouse monoclonal antibody was used to counterstain at 1/200 dilution, followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at 1 : 1000 dilution (Magenta).
-ve control 1 : ab325526 at 1/200 dilution, followed by ab150120 at 1/1000 dilution.
-ve control 2 : anti-KDEL at 1/200 dilution, followed by ab150081 at 1/1000 dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human testis tissue labeling CISD2 with ab325526 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human testis. The primary antibody was incubated 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
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human colon carcinoma tissue labeling CISD2 with ab325526 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human colon carcinoma. The primary antibody was incubated 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
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling CISD2 with ab325526 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human kidney. The primary antibody was incubated 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
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse lung carcinoma tissue labeling CISD2 with ab325526 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse lung carcinoma. The primary antibody was incubated 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
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling CISD2 with ab325526 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse kidney (PMID : 33916457). The primary antibody was incubated 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
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling CISD2 with ab325526 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse cerebrum. The primary antibody was incubated 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
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 100% methanol-fixed, 0.1% TritonX-100 permeabilized C2C12 (mouse myoblast) cells labelling CISD2 with ab325526 at 1/200 (2.495 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Confocal image showing cytoplasmic staining in C2C12 cells (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-KDEL mouse monoclonal antibody was used to counterstain tubulin at 1/200 dilution, followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at 1 : 1000 dilution (Magenta).
-ve control 1 : ab325526 at 1/200 dilution, followed by ab150120 at 1/1000 dilution.
-ve control 2 : anti-KDEL at 1/200 dilution, followed by ab150081 at 1/1000 dilution.
- WB
Lab
Western blot - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Exposure time : Lane1-3 : 8 seconds, lane 4 : 3 seconds
All lanes:
Western blot - Anti-CISD2 antibody [EPR30277-16] (<a href='/en-us/products/primary-antibodies/cisd2-antibody-epr30277-16-ab325526'>ab325526</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervical adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 3:
C2C12 (mouse myoblast) whole cell lysate at 20 µg
Lane 4:
PC-12 (rat adrenal gland pheochromocytoma cell) 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
Observed band size: 15 kDa
false
- WB
Lab
Western blot - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Lanes 1-4 are incubated with Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 and lanes 5-6 are incubated with Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/100000.
Exposure time : Lane1-4 : 3 seconds, lane 5-6 : 10 seconds
All lanes:
Western blot - Anti-CISD2 antibody [EPR30277-16] (<a href='/en-us/products/primary-antibodies/cisd2-antibody-epr30277-16-ab325526'>ab325526</a>) at 1/1000 dilution
Lane 1:
Human testis tissue lysate at 20 µg
Lane 2:
Human lung tissue lysate at 20 µg
Lane 3:
Mouse testis tissue lysate at 20 µg
Lane 4:
Mouse brain tissue lysate at 20 µg
Lane 5:
Rat testis tissue lysate at 20 µg
Lane 6:
Rat brain tissue lysate at 20 µg
Secondary
Lanes 1 - 4:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Lanes 5 - 6:
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: 15 kDa
false
- WB
Lab
Western blot - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with human CISD1 by western blot.
In Western blot, Anti-6X His tag® antibody [AD1.1.10] - (ab15149) (1 : 1000) (60KDa).
false
Exposure time: 26s
- WB
Lab
Western blot - Anti-CISD2 antibody [EPR30277-16] - BSA and Azide free (AB325533)
This data was developed using ab325526, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-CISD2 antibody [EPR30277-16] (<a href='/en-us/products/primary-antibodies/cisd2-antibody-epr30277-16-ab325526'>ab325526</a>) at 1/1000 dilution
Lane 1:
HEK-293 (human embryonic kidney epithelial cell) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2:
HEK-293 transfected with siRNA specifically targeting CISD2 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
Observed band size: 15 kDa,36 kDa
false
Exposure time: 37s
Reactivity data
Product details
ab325533 is the carrier-free version of ab325526
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
- Visit the General protocols
- Visit the Troubleshooting
Target data
Additional targets
Product promise
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