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Anti-RUNX2 Antibody (4W937) 是一种 Rabbit 抗体,靶向 RUNX2。Anti-RUNX2 Antibody (4W937) 可用于 ICC/IF,IHC,WB。
Anti-RUNX2 Antibody (4W937) 是一种 Rabbit 抗体,靶向 RUNX2。Anti-RUNX2 Antibody (4W937) 可用于 ICC/IF,IHC,WB。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
50 μL | ¥ 1,485 | 5日内发货 | |
100 μL | ¥ 2,485 | 5日内发货 |
产品描述 | Anti-RUNX2 Antibody (4W937) is a Rabbit antibody targeting RUNX2. Anti-RUNX2 Antibody (4W937) can be used in ICC/IF,IHC,WB. |
别名 | SL3/AKV core binding factor alpha A subunit, SL3 3 enhancer factor 1 alpha A subunit, RUNX 2, Runt-related Transcription Factor 2, Runt related transcription factor 2, Runt domain, Polyomavirus enhancer binding protein 2 alpha A subunit, PEBP2-alpha A, PEBP2aA1, PEBP2A2, PEBP2A1, PEBP2 alpha A, PEA2aA, PEA2 alpha A, OTTHUMP00000016533, Osteoblast specific transcription factor 2, OSF2, OSF 2, Oncogene AML 3, MGC120023, Core binding factor subunit alpha 1, Core binding factor runt domain alpha subunit 1, Core binding factor, Cleidocranial dysplasia 1, CLCD, CCD1, CCD, CBFA1, CBF alpha 1, AML3 |
Ig Type | IgG |
交叉反应 | Human,Mouse,Rat |
验证活性 | 1. Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-RUNX2 antibody. Counter stained with hematoxylin. 2. ICC staining RUNX2 in SW480 cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
应用 | |
推荐剂量 | WB: 1:1000; IHC: 1:50-200; ICC/IF: 1:50-200 |
抗体种类 | Monoclonal |
宿主来源 | Rabbit |
构建方式 | Recombinant Antibody |
纯化方式 | ProA affinity purified |
性状 | Liquid |
缓冲液 | 1*TBS (pH7.4), 1%BSA, 40%Glycerol. Preservative: 0.05% Sodium Azide. |
研究背景 | The mammalian Runt-related transcription factor (RUNX) family comprises three members, RUNX1 (also designated AML-1, PEBP2αB, CBFA2), RUNX2 (also designated AML-3, PEBP2αA, CBFA1, Osf2) and RUNX3 (also designated AML-2, PEBPαC, CBFA3). RUNX family members are DNA-binding proteins that regulate the expression of genes involved in cellular differentiation and cell cycle progression. RUNX2 is essential for skeletal mineralization in that it stimulates osteoblast differentiation of mesenchymal stem cells, promotes chondrocyte hypertrophy and contributes to endothelial cell migration and vascular invasion of developing bones. Regulating RUNX2 expression may be a useful therapeutic tool for promoting bone formation. Mutations in the C-terminus of RUNX2 are associated with cleidocranial dysplasia syndrome, an autosomal-dominant skeletal dysplasia syndrome that is characterized by widely patent calvarial sutures, clavicular hypoplasia, supernumerary teeth, and short stature. |
偶联 | Unconjugated |
免疫原 | Recombinant Protein |
Uniprot ID |
储存方式 | Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
运输方式 | Shipping with blue ice. |
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