Application
Formalin fixed paraffin embedded human lymph node stained with Hairy Cell Leukemia antibody .| Product Name | Hairy Cell Leukemia antibody (ready-to-use) |
|---|---|
| Antibody Type | Primary Antibodies |
| Product description | Mouse monoclonal [DBA.44] to Hairy Cell Leukemia prediluted |
| Immunogen | BALB/C mice were injected with the Deau cell line established from alla large cell lymphoma. |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgM |
| Clone Number | DBA.44 |
| Host Species | Mouse |
| Tested Applications | IHC-FIHC-P |
| This antibody has been pretitered and quality controlled to work allon formalin-fixed paraffin-embedded as well as acetone fixed cryostat tissue sections. No further titration is required. We suggest an incubation period of 30-60 minutes at room temperature. However, depending upon the fixation conditions and the staining system employed, optimal incubation should be determined by the user. Enzymatic predigestion with proteolytic enzymes should be performed before the immunostaining.cryostat tissue sections. Optimal dilutions/concentrations should be determined by the researcher.: |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Gene Synonyms | CDK105 HCL-G1 HCLG1 HUSSY29 TINP1 YR-29 YR 29 HCL G1 YR29 |
|---|---|
| Target | Hairy Cell Leukemia |
| Tissue Specificity | This antibody reacts with over 97% of hairy cell leukaemias as well as about 35% of high grade B cell lymphomas. It reacts with B lymphocytes, cells of mantle zone and immunoblasts outside the lymphoid tissues. |
| Light Chain Type | kappa |
Application
Formalin fixed paraffin embedded human lymph node stained with Hairy Cell Leukemia antibody .| Positive Control | Tonsil |
|---|---|
| Application Notes | This antibody has been pretitered and quality controlled to work allon formalin-fixed paraffin-embedded as well as acetone fixed cryostat tissue sections. No further titration is required. We suggest an incubation period of 30-60 minutes at room temperature. However, depending upon the fixation conditions and the staining system employed, optimal incubation should be determined by the user. Enzymatic predigestion with proteolytic enzymes should be performed before the immunostaining.cryostat tissue sections. Optimal dilutions/concentrations should be determined by the researcher.: |
| Form | Liquid |
|---|---|
| Storage Instructions | Keep as concentrated solution, aliquot and store at 4°C. Do not freeze. |
| Storage Buffer | Phosphate-buffered saline containing sodium azide |
