hnRNP M Mouse Monoclonal Antibody(C2748)
MSDS 
Key features and details
- Target:
- Source/Host:
- Reactivity:
- Clonality:
- Applications:
- Conjugation:
- Storage:
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Brand:
Product Details
WB | 1:500 - 1:1000 |
IHC | 1:100 - 1:500 |
IF/ICC | 1:100 - 1:500 |
FC | 1:100 - 1:200 |
Description | Mouse monoclonal to hnRNP M |
Specificity | Recognizes endogenous levels of hnRNP M protein |
Antibody Type | Primary antibody |
Imnunogen | Recombinant fusion protein of human hnRNP M expressed in E. Coli |
Purification | This antibody is purified through a protein G column. |
Molecular Weight | Predicted: 78 kD; Observed: 80 kD kD |
Form/Buffer | Mouse IgG1. Liquid in PBS, pH 7.3, 30% glycerol, and 0.01% sodium azide. |
Alternative Names | HNRPM; NAGR1; Heterogeneous nuclear ribonucleoprotein M; hnRNP M |
Gene Symbol | HNRNPM |
Entrez Gene | 4670(Human); 76936(Mouse); 116655(Rat) |
SwissProt | P52272(Human); Q9D0E1(Mouse); Q62826(Rat) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.
Western blot analysis of hnRNP M expression in Raji (A), Hela (B), NIH/3T3 (C), A431 (D), A549 (E), HepG2 (F), PC12 (G), U251 (H) whole cell lysates. (Predicted band size: 78 kD; Observed band size: 80 kD kD)
Immunohistochemical analysis of hnRNP M staining in human esophageal cancer formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Immunofluorescent analysis of hnRNP M staining in Hela cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with an AREX® Fluor 488 -conjugated secondary antibody (green) in PBS at room temperature in the dark. Phalloidin - AREX® Fluor 594 was used to stain Actin filaments (red). DAPI was used to stain the cell nuclei (blue).
Flow cytometric analysis of HL60 cells using Anti-hnRNP M Antibody (green) and negative control (red).
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