Abeomics/β肌动蛋白多克隆抗体/25µg/11-13012-免疫在线蚂蚁淘旗下平台

商品详细Abeomics/β肌动蛋白多克隆抗体/25µg/11-13012

Abeomics/β肌动蛋白多克隆抗体/25µg/11-13012

商品编号： 11-13012

品牌： Abeomics

市场价： ¥1600.00

美元价： 800.00

产地：美国(厂家直采)

公司：

产品分类：免疫组化试剂盒

公司分类： Immunostain_SP_Kit

联系Q Q： 3392242852

电话号码： 4000-520-616

电子邮箱： info@ebiomall.com

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商品介绍

Format :	Purified
Amount :	100 µg
Isotype :	Rabbit IgG
Purification :	Protein A Chromatography
Content :	25 µg in 50 µl/100 µg in 200 µl PBS containing 0.05% BSA and 0.05% sodium azide. Sodium azide is highly toxic.
Storage condition :	Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.


Gene :	ACTB
Gene ID :	60
Uniprot ID :	P60709
Alternative Name :	Actin, cytoplasmic 1, ACTB
Immunogen Information :	A partial length recombinant Beta actin protein (amino acids 1-200) was used as the immunogen for this antibody.

B-actin (ACTB) has traditionally been regarded as an endogenous housekeeping gene and has been widely used as a reference gene/protein in quantifying expression levels in tumors. It supports fundamental cellular processes in healthy and diseased cells including cell adhesion, migration, cytokinesis and maintenance of cell polarity. However, B-actin is closely associated with a variety of cancers and accumulating evidence indicates that B-actin is de-regulated in liver, melanoma, renal, colorectal, gastric, pancreatic, esophageal, lung, breast, prostate, ovarian cancers, leukemia and lymphoma. This protein is generally found to be up-regulated in the majority of tumor cells and tissues.

Western blot analysis: 4-6 µg/ml:

For Research Use Only. Not for use in diagnostic/therapeutics procedures.

1. Panda PK, Naik PP, Meher BR, Das DN, Mukhopadhyay S, Praharaj PP, Maiti TK,Bhutia SK. PUMA dependent mitophagy by Abrus agglutinin contributes to apoptosis through ceramide generation. Biochim Biophys Acta Mol Cell Res. 2018Mar;1865(3):480-495. doi: 10.1016/j.bbamcr.2017.12.002. Epub 2017 Dec 8. PubMedPMID: 2922947

2. Nayak TK, Mamidi P, Kumar A, Singh LP, Sahoo SS, Chattopadhyay S,Chattopadhyay S. Regulation of Viral Replication, Apoptosis and Pro-Inflammatory Responses by 17-AAG during Chikungunya Virus Infection in Macrophages. Viruses.2017 Jan 6;9(1). pii: E3. doi: 10.3390/v9010003. PubMed PMID: 28067803; PubMedCentral PMCID: PMC5294972.

3. Panigrahi B, Singh RK, Mishra S, Mandal D. Cyclic peptide-based nanostructuresas efficient siRNA carriers. Artif Cells Nanomed Biotechnol. 2018 Oct 12:1-11.doi: 10.1080/21691401.2018.1511574. [Epub ahead of print] PubMed PMID: 30311806.

4. Panigrahi B, Mishra S, Singh RK, Siddiqui N, Bal R, Mandal D. Peptidegenerated anisotropic gold nanoparticles as efficient siRNA vectors. Int J Pharm.2019 May 30;563:198-207. doi: 10.1016/j.ijpharm.2019.04.007. Epub 2019 Apr 3.PubMed PMID: 30953762.

5. Yavvari PS, Verma P, Mustfa SA, Pal S, Kumar S, Awasthi AK, Ahuja V, Srikanth CV, Srivastava A, Bajaj A. A nanogel based oral gene delivery system targetingSUMOylation machinery to combat gut inflammation. Nanoscale. 2019 Mar14;11(11):4970-4986. doi: 10.1039/c8nr09599j. PubMed PMID: 30839018.

6. Shahror RA, Linares G, Wang Y, Hsueh SC, Wu CC, Chuang DM, Chiang YH, Chen KY.Transplantation of Mesenchymal Stem Cells Overexpressing FGF21 FacilitatesCognitive Recovery and Enhances Neurogenesis in a Mouse Model of Traumatic Brain Injury. J Neurotrauma. 2019 Jul 12. doi: 10.1089/neu.2019.6422. [Epub ahead ofprint] PubMed PMID: 31298621.

Subcellular location:	Cytoplasm, Nucleus
Post transnational modification:	(Microbial infection) Monomeric actin is cross-linked by V.cholerae toxins RtxA and VgrG1 in case of infection: bacterial toxins mediate the cross-link between Lys-50 of one monomer and Glu-270 of another actin monomer, resulting in formation of highly toxic actin oligomers that cause cell rounding (PubMed:19015515). The toxin can be highly efficient at very low concentrations by acting on formin homology family proteins: toxic actin oligomers bind with high affinity to formins and adversely affect both nucleation and elongation abilities of formins, causing their potent inhibition in both profilin-dependent and independent manners (PubMed:26228148).
BioGrid:	106575.336 interactions.

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