BCL9 Rabbit pAb
- 产品详情
- 实验流程
Application
| WB, IHC-P, IHC-F, IF, E |
|---|---|
| Primary Accession | O00512 |
| Other Accession | O00512 |
| Host | Rabbit |
| Clonality | Polyclonal |
| Calculated MW | 149290 Da |
| Physical State | Liquid |
| Immunogen | KLH conjugated synthetic peptide derived from human BCL9 |
| Epitope Specificity | 51-150/1426 |
| Isotype | IgG |
| Purity | affinity purified by Protein A |
| Buffer | 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol. |
| SIMILARITY | Belongs to the BCL9 family. |
| SUBUNIT | Binds to beta-catenin (CTNNB1), PYGO1 and PYGO2. |
| Post-translational modifications | Phosphorylated upon DNA damage, probably by ATM or ATR. |
| DISEASE | Note=A chromosomal aberration involving BCL9 is found in a patient with precusor B-cell acute lymphoblastic leukemia (ALL). Translocation t(1;14)(q21;q32). This translocation leaves the coding region intact, but may have pathogenic effects due to alterations in the expression level of BCL9. Several cases of translocations within the 3'-UTR of BCL9 have been found in B-cell malignancies. |
| Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications. |
| Background Descriptions | Bcl-9L is a 1,499 amino acid protein that localizes to the nucleus and contains a specialized C-terminal domain that is important for its overall activity. Expressed in breast tissue, as well as in eye, lung, prostate and various carcinomas, Bcl-9L functions as a transcriptional activator that forms a complex with Parafibromin and β-catenin and is thought promote the transcriptional activity of Parafibromin and enhance the neoplastic transforming activity of β-catenin. Bcl-9L exists as multiple alternatively spliced isoforms and is thought to be involved in tumorigenesis, possibly playing a role in tumor transformation and metastasis. The gene encoding Bcl-9L maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11. |
| Gene ID | 607 |
|---|---|
| Other Names | LGS; 2610202E01Rik; 8030475K17Rik; A330041G23Rik; Gm130; BCL9_HUMAN; BCL9; B-cell lymphoma 9 protein; Bcl-9; Protein legless homolog; Q1JQ81_HUMAN; Q5T489_HUMAN; BCL9_MOUSE; BCL9 transcription coactivator; B cell CLL/lymphoma 9; BCL9, transcription coactivator |
| Dilution | WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,ELISA=1:5000-10000 |
| Storage | Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C. |
For Research Use Only. Not For Use In Diagnostic Procedures.
| Name | BCL9 |
|---|---|
| Function | Involved in signal transduction through the Wnt pathway. Promotes beta-catenin's transcriptional activity (By similarity). |
| Cellular Location | Nucleus. |
| Tissue Location | Detected at low levels in thymus, prostate, testis, ovary and small intestine, and at lower levels in spleen, colon and blood |
Research Areas
Application Protocols
Provided below are standard protocols that you may find useful for product applications.
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