Antibodi Poliklonal Kelinci RUNX2
WB | 1:500 - 1:1000 |
IHC | 1:50 - 1:100 |
JIKA/ICC | 1:50 - 1:100 |
Deskripsi | Antibodi poliklonal kelinci terhadap RUNX2 |
Kekhususan | Mengenali tingkat protein RUNX2 endogen. |
Tipe Antibodi | Antibodi primer |
Imunogen | Protein rekombinan yang sesuai dengan RUNX2 manusia. Urutan persisnya adalah hak milik. |
Pemurnian | Antibodi dimurnikan dengan kromatografi afinitas imunogen. |
Berat Molekul | Prediksi: 54; Diamati: 60 kD |
Formulir/Penyangga | Cairan dalam 0,42% Kalium fosfat, 0,87% Natrium klorida, pH 7,3, 30% gliserol, dan 0,01% natrium azida. |
Nama Alternatif | AML3; CBFA1; OSF2; PEBP2A; Runt-related transcription factor 2; Acute myeloid leukemia 3 protein; Core-binding factor subunit alpha-1; CBF-alpha-1; Oncogene AML-3; Osteoblast-specific transcription factor 2; OSF-2; Polyomavirus enhancer-binding protein 2 alpha A subunit; PEA2-alpha A; PEBP2-alpha A; SL3-3 enhancer factor 1 alpha A subunit; SL3/AKV core-binding factor alpha A subunit |
Simbol Gen | RUNX2 |
Entrez Gene | 860(Manusia); 12393 (Tikus) |
SwissProt | Q13950(Manusia); Q08775(Tikus); Q9Z2J9(Tikus) |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

Western blot analysis of RUNX2 expression in Hela (A), mouse testis (B) whole cell lysates. (Predicted band size: 54; 55; 56 kD; Observed band size: 60 kD)

Immunohistochemical analysis of RUNX2 staining in rat spleen 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 RUNX2 staining in rat spleen. 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 humidified chamber. Cells were washed with PBST and incubated with a AREX® Fluor 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).
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