Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free
- BOND RX™ Validated
- RabMAb
- Recombinant
- What is this?
Be the first to review this product! Submit a review
|
(0 Publication)
Rabbit Recombinant Monoclonal YTHDC2 antibody. Carrier free. Suitable for IP, WB, IHC-Fr, IHC-P and reacts with Human, Mouse, Rat samples.
View Alternative Names
3'-5' RNA helicase YTHDC2, YTH domain-containing protein 2, hYTHDC2, YTHDC2
- IP
Supplier Data
Immunoprecipitation - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
YTHDC2 was immunoprecipitated from 0.35 mg HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10 μg with ab271139 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab271139 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate 10 μg
Lane 2 : ab271139 IP in HeLa whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab271139 in HeLa whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 24 seconds.
Lysates were made freshly and used in IP test immediately to minimize protein degradation.
All lanes:
Immunoprecipitation - Anti-YTHDC2 antibody [EPR24278-9] (<a href='/en-us/products/primary-antibodies/ythdc2-antibody-epr24278-9-ab271139'>ab271139</a>)
Predicted band size: 160 kDa
Observed band size: 160 kDa
false
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labelling YTHDC2 with ab271139 at 1/2000 (0.285 μg/mL) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on mouse cerebrum. The section was incubated with ab271139 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse heart (fresh) tissue labeling YTHDC2 with ab271139 at 1/50 (11.4 μg/mL) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). The nuclear counterstain was DAPI (Blue).
No staining on mouse heart
Negative control : (PMID : 29087293)
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat testis tissue labelling YTHDC2 with ab271139 at 1/2000 (0.285 μg/mL) followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection) was used. Cytoplasmic staining on rat testis. The section was incubated with ab271139 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse testis (fresh) tissue labeling YTHDC2 with ab271139 at 1/50 (11.4 μg/mL) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). Cytoplasmic staining on mouse testis 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 at 1/1000 dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat testis (fresh) tissue labeling YTHDC2 with ab271139 at 1/50 (11.4 μg/mL) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). Cytoplasmic staining on rat testis is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 dilution.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat heart (fresh) tissue labeling YTHDC2 with ab271139 at 1/50 (11.4 μg/mL) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green). The nuclear counterstain was DAPI (Blue).
No staining on rat heart
Negative control : (PMID : 29087293)
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labelling YTHDC2 with ab271139 at 1/2000 (0.285 μg/mL) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on rat cerebrum. The section was incubated with ab271139 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 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-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse testis tissue labelling YTHDC2 with ab271139 at 1/2000 (0.285 μg/mL) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). Cytoplasmic staining on mouse testis (PMID : 28809393). The section was incubated with ab271139 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 with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IP
Supplier Data
Immunoprecipitation - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
YTHDC2 was immunoprecipitated from 0.35 mg RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate 10 μg with ab271139 at 1/30 dilution (2μg in 0.35mg lysates). Western blot was performed on the immunoprecipitate using ab271139 at 1/1000 dilution. VeriBlot for IP secondary antibody(HRP) (ab131366) was used at 1/5000 dilution.
Lane 1 : RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate 10μg
Lane 2 : ab271139 IP in RAW264.7 whole cell lysate
Lane 3 : Rabbit monoclonal IgG (ab172730) instead of ab271139 in RAW264.7 whole cell lysate
Blocking and dilution buffer and concentration : 5% NFDM/TBST.
Exposure time : 67 seconds.
Lysates were made freshly and used in IP test immediately to minimize protein degradation.
All lanes:
Immunoprecipitation - Anti-YTHDC2 antibody [EPR24278-9] (<a href='/en-us/products/primary-antibodies/ythdc2-antibody-epr24278-9-ab271139'>ab271139</a>)
Predicted band size: 160 kDa
Observed band size: 160 kDa
false
- WB
Lab
Western blot - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Lysates were made freshly and used in WB test immediately to minimize protein degradation.
Exposure time : Lane 1-2, 4-5 : 37 seconds. Lane 3 : 3 minutes.
All lanes:
Western blot - Anti-YTHDC2 antibody [EPR24278-9] (<a href='/en-us/products/primary-antibodies/ythdc2-antibody-epr24278-9-ab271139'>ab271139</a>) at 1/1000 dilution
Lane 1:
HeLa (human cervix adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 3:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 4:
PC-12 (rat adrenal gland pheochromocytoma) whole cell lysate at 20 µg
Lane 5:
RAW264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) 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: 160 kDa
Observed band size: 160 kDa
false
- WB
Lab
Western blot - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST
The observed MW & expression profile are consistent with what has been described in the literature (PMID : 29799838, PMID : 29087293).
Low expression : heart (PMID : 29799838, PMID : 29087293).
Exposure time : 15 seconds.
All lanes:
Western blot - Anti-YTHDC2 antibody [EPR24278-9] (<a href='/en-us/products/primary-antibodies/ythdc2-antibody-epr24278-9-ab271139'>ab271139</a>) at 1/1000 dilution
Lane 1:
Mouse testis tissue lysate at 20 µg
Lane 2:
Mouse heart tissue 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: 160 kDa
Observed band size: 160 kDa
false
- WB
Lab
Western blot - Anti-YTHDC2 antibody [EPR24278-9] - BSA and Azide free (AB283277)
This data was developed using ab271139, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
The observed MW & expression profile are consistent with what has been described in the literature (PMID : 29799838, PMID : 29087293).
Low expression : heart (PMID : 29799838, PMID : 29087293).
Exposure time : 114 seconds.
All lanes:
Western blot - Anti-YTHDC2 antibody [EPR24278-9] (<a href='/en-us/products/primary-antibodies/ythdc2-antibody-epr24278-9-ab271139'>ab271139</a>) at 1/1000 dilution
Lane 1:
Rat testis tissue lysate at 20 µg
Lane 2:
Rat heart tissue 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: 160 kDa
Observed band size: 160 kDa
false
Related conjugates and formulations (1)
-
Anti-YTHDC2 antibody [EPR24278-9]
Reactivity data
Product details
ab283277 is the carrier-free version of ab271139.
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
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
YTHDC2 contributes to the regulation of mRNA stability and turnover within the cell. It may operate as part of a complex involved in post-transcriptional control. Through these actions YTHDC2 influences processes such as meiosis and the differentiation of germ cells supported by its association with m6A reader proteins. This association plays a role in the recognition of specific m6A marks critical for RNA dynamics.
Pathways
YTHDC2 integrates into the m6A-dependent RNA decay and translation machinery. One important pathway involving this protein is the m6A-mediated gene expression regulation pathway. Within this context YTHDC2 interacts closely with other m6A machinery components such as METTL3 and bridges mRNA modification with subsequent cellular outcomes. Another related pathway is spermatogenesis where the precise control by YTHDC2 is necessary for successful meiosis via interaction with various meiotic proteins.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
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