抗体

MDM2 (E3 Ubiquitin-protein Ligase Mdm2, Double Minute 2 Protein, Hdm2, Oncoprotein Mdm2, p53-binding Protein Mdm2)

M2800-05

50微克

535美元

单克隆

小鼠

未共轭

3G187

MDM2 (E3 Ubiquitin-protein Ligase Mdm2, Double Minute 2 Protein, Hdm2, Oncoprotein Mdm2, p53-binding Protein Mdm2)

小鼠

单克隆抗体

抗体

50微克

535美元

3G187

IgG2b, k

The MDM2 (murine double minute 2) proto-oncogene was originally identified as an amplified gene in a mouse tumor cell line. Overexpression of MDM2 was shown to produce tumors in athymic mice. In a separate set of studies, the 90kD MDM2 was found to bind and inactivate the transcriptional activity of the p53 protein. p53 was also identified as the major target for MDM2 during embryonic development by virtue of the fact that the lethal effects produced by knocking out MDM2 could be reversed by the simultaneous deletion of p53. The MDM2 gene itself is a transcriptional target for p53, and induction of p53 transcriptional activity results in increased MDM2 mRNA and protein levels. It appears that a MDM2 p53 feedback loop serves to keep the growth suppressive functions of p53 in check during the normal cell cycle. Recent studies have implicated MDM2 in regulating cell proliferation via p53-independent pathways. This is based on evidence that MDM2 can interact with Rb, E2F-1 and DP1. Applications: Suitable for use in Immunofluorescence/Immunocytochemistry, Western Blot, Immunoprecipitation and Immunohistochemistry. Other applications not tested. Recommended Dilutions: Immunofluorescence (IC): 1:25-1:200 Western Blot: 0.5-2ug/ml (ECL) See publication #1 Immunohistochemistry: Frozen See publication #7 Immunohistochemistry (Paraffin): 1:25-1:200. Requires heat induced epitope retrieval pretreatment. Used to characterize a primary myxoid liposarcoma with chondroid and osseous components (ref.11). See publication #1, 2, 7 Immunoprecipitation: 1-5ug/ml Optimal dilutions to be determined by the researcher. Positive Controls: OsA-CL, MCF-7, HeLa cell lysates Negative Control: HOS cells Storage and Stability: May be stored at 4°C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20°C. Aliquots are stable for 12 months after receipt. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

Hu

HDMX; ACTFS; hdm2; p53 E3 ubiquitin protein ligase homolog, Mdm2; transformed 3T3 cell double minute 2; p53 binding protein; MGC5370; MGC71221

Synthetic peptide corresponding to the N-terminal of human MDM2. Epitope: aa26-169. Species Sequence Homology: bacteria, guinea pig, rat.

Recognizes human MDM2 at ~90kD. Also recognizes isoforms at ~57 and ~74/76kD.

Purified by Protein A affinity chromatography.

以溶解在PBS液体方式提供, pH值7.4, 1毫克/毫升BSA, 0.05% 叠氮化钠, 30% 甘油

~0.5毫克/毫升

Product Type: Mab Isotype: IgG2b,k Clone No: 3G187 Host: mouse Source: human Concentration: ~0.5mg/ml Form: Supplied as a liquid in PBS, pH 7.4, 1mg/ml BSA, 0.05% sodium azide, 30% glycerol. Purity: Purified by Protein A affinity chromatography. Immunogen: Synthetic peptide corresponding to the N-terminal of human MDM2. Epitope: aa26-169. Species Sequence Homology: bacteria, guinea pig, rat. Specificity: Recognizes human MDM2 at ~90kD. Also recognizes isoforms at ~57 and ~74/76kD. Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.

细胞化学IF免疫组化免疫沉淀免疫印迹

-20°C

1. Leach, F. S., et al, Cancer Res. 53: 2231–2234 (1993). 2. Oliner, J.D. et. al., Nature, 358: 80–83 (1992). 3. Momand, J. et al, Cell, 69: 1237–1245 (1992). 4. Barak, Y., et al, EMBO J. 12: 461–468 (1993). 5. Marchetti, A., et al, J. Pathol. 175: 31–38 (1995). General 6. Cahilly-Snyder, L., et al., Somat. Cell Mol. Genet. 13: 235–234 (1987). 7. Fakharzadeh, S.et al, EMBO J., 10: 1565–1569 (1991). 8. Haines, D.S., et. al., Leuk. Lymphoma 26: 227–238 (1997). 9. Momand, J., et al., Nucleic Acids Res. 26: 3453–3459 (1998). 10. Oliner, J.D., et al., Nature 362: 857–860 (1993). 11. Weingertner N, et al., Applied immunohistochemistry & Molecular Morphology: 23:230 (2015).

https://usbio-images.r.worldssl.net/prodimages/7/M2800-05_1.jpg