IF
IF analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish embryo tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:100. Fluoro488 Conjugated Goat Anti-Rabbit IgG was used as secondary antibody.WB
Western blot analysis of HNRNPD using anti-HNRNPD antibody . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: zebrafish embryo tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HNRNPD antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody . The signal is developed using ECL Plus Western Blotting Substrate . A specific band was detected for HNRNPD at approximately 40 kDa. The expected band size for HNRNPD is at 38 kDa.IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish cerebellum tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish heart tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish colon tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish muscle tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.| Product Name | Anti-Zebrafish HNRNPD Antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Immunogen | E.coli-derived zebrafish HNRNPD recombinant protein (Position: K43-N203) |
| Clonality | Polyclonal |
|---|---|
| Isotype | IgG |
| Host Species | Rabbit |
| Tested Applications | IFWBIHC |
| WB:1:500-1:2000 IHC:1:50-1:400 IF:1:50-1:400 |
|
| Species Reactivity | Zebrafish |
| Concentration | 500ug/ml |
| Purification | Affinity purified |
| Target | HNRNPD |
|---|---|
| Alternative Names | AUF1 AUF1A hnRNP D0 HNRNPD hnRNPD0 HNRPD P37 |
| Molecular Weight(MW) | 38 kDa(Observed band size: 40 kDa) |
| SwissProt ID | A0A8M9QC46 |
|---|
IF
IF analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish embryo tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:100. Fluoro488 Conjugated Goat Anti-Rabbit IgG was used as secondary antibody.
WB
Western blot analysis of HNRNPD using anti-HNRNPD antibody . The sample well of each lane was loaded with 30 ug of sample under reducing conditions.Lane 1: zebrafish embryo tissue lysates.After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HNRNPD antigen affinity purified polyclonal antibody at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody . The signal is developed using ECL Plus Western Blotting Substrate . A specific band was detected for HNRNPD at approximately 40 kDa. The expected band size for HNRNPD is at 38 kDa.
IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish brain tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish cerebellum tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish heart tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish colon tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.
IHC
IHC analysis of HNRNPD using anti-HNRNPD antibody .HNRNPD was detected in a paraffin-embedded section of zebrafish muscle tissue. The tissue section was incubated with rabbit anti-HNRNPD Antibody at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit with DAB as the chromogen.| Application Notes | WB:1:500-1:2000 IHC:1:50-1:400 IF:1:50-1:400 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | 12 months from date of receipt,-20℃ as supplied. |
| Storage Buffer | PBS, 0.02% NaN3, 1 mg/ml BSA and 50% glycerol. |
