Thermo Fisher 711087 抗体,TBX3 Recombinant Polyclonal Antibody (22HCLC)/TBX3重组多克隆抗体(22HCLC)

2024-10-23

TBX3 Recombinant Polyclonal Antibody (22HCLC)/TBX3重组多克隆抗体(22HCLC)

货号:711087

规格:100 µg

价格:4809

产品类型:抗体和染料

品牌:Thermo Fisher

抗原:Protein corresponding to Human TBX3 (aa 305-500)

物种:人

宿主:兔

抗体亚型:IgG

克隆号:22HCLC

荧光染料:其它

类型:多抗同型对照:
浓度: 0.5 mg/mL用法:2.5 µg x 10^6 cells(ChIP);2 µg/mL(ICC);2 µg/mL(IF)
产品详细信息This antibody is predicted to react with Monkey, Pig and RatRecombinant rabbit polyclonal antibodies are unique offerings from Thermo Fisher Scientific. They are comprised of a selection of multiple different recombinant monoclonal antibodies, providing the best of both worlds - the sensitivity of polyclonal antibodies with the specificity of monoclonal antibodies - all delivered with the consistency only found in a recombinant antibody. While functionally the same as a polyclonal antibody - recognizing multiple epitope sites on the target and producing higher detection sensitivity for low abundance targets - a recombinant rabbit polyclonal antibody has a known mixture of light and heavy chains. The exact population can be produced in every lot, circumventing the biological variability typically associated with polyclonal antibody production.靶标信息T-box 3 (TBX3) is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. The Tbx3 protein is a transcriptional repressor that binds the canonical Brachychury bindig sites, and is thought to play a role in the anterior/posterior axis of the tetrapod forelimb. Tbx3 is required for normal mammary development and is also implicated in tumor development.Tbx3 expression also increases during osteoblast differentiation, and may function as a determinant of osteoblast cell numbers. Mutations in T-box 3 cause ulnar-mammary syndrome (MIM 181450), affecting limb, apocrine gland, tooth, hair, and genital development. Alternative splicing results in three transcript variants encoding different isoforms; however, the nature of one full length variant has not been determined. Subsets of human breast cancer cell lines overexpress TBX36. in vitro, Tbx3 overexpression in mouse embryo fibroblasts leads to immortalization of cells. Truncated forms of Tbx3 are increased in plasma samples.

数据:
TBX3 Antibody (711087) in IFFor immunofluorescence analysis, MCF7 cells were fixed and permeabilized for detection of endogenous TBX3 using Anti- TBX3 Recombinant Rabbit Polyclonal Antibody (Product # 711087, 2 µg/mL) and labeled with Goat anti-Rabbit IgG (H+L) Superclonal Secondary Antibody, Alexa Fluor® 488 conjugate (Product # A27034, 1:2000). Panel a) shows representative cells that were stained for detection and localization of TBX3 protein (green), Panel b) is stained for nuclei (blue) using SlowFade® Gold Antifade Mountant with DAPI (Product # S36938). Panel c) represents cytoskeletal F-actin staining using Alexa Fluor® 555 Rhodamine Phalloidin (Product # R415, 1:300). Panel d) is a composite image of Panels a, b and c clearly demonstrating nuclear localization of TBX3. Panel e) represents control cells with no primary antibody to assess background. The images were captured at 60X magnification.

TBX3 Antibody (711087) in ChIPEnrichment of endogenous TBX3 protein at specific gene loci using Anti-TBX3 Recombinant Rabbit Polyclonal Antibody: Chromatin Immunoprecipitation (ChIP) was performed using Anti-TBX3 Recombinant Rabbit Monoclonal Antibody (Product # 711087, 5 µg) on sheared chromatin from 2 million HEPG2 cells using the "MAGnify ChIP system" kit (Product # 49-2024). Normal Rabbit IgG (1 µg) was used as a negative IP control. The purified DNA was analyzed by 7500 Fast qPCR system (Product # 4351106) with optimized PCR primer pairs for the different loci of the active P21 promoter region used as positive control target genes, and the region of the inactive MYOD, SAT2 satellite repeat, used as negative control target gene. Data is presented as fold enrichment of the antibody signal versus the negative control IgG using the comparative CT method.
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