CCT6B Rabbit Pab

Total Page：16

File Type：pdf, Size：1020Kb

Leader in Biomolecular Solutions for Life Science CCT6B Rabbit pAb Catalog No.: A14615 1 Publications Basic Information Background Catalog No. This gene encodes a molecular chaperone that is a member of the chaperonin- A14615 containing TCP1 complex (CCT), also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings, each containing eight different proteins. Observed MW Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP- 58kDa dependent manner. The complex folds various proteins, including actin and tubulin. Alternative splicing results in multiple transcript variants. Calculated MW 53kDa/57kDa Category Primary antibody Applications WB,IF Cross-Reactivity Human, Mouse, Rat Recommended Dilutions Immunogen Information WB 1:500 - 1:2000 Gene ID Swiss Prot 10693 Q92526 IF 1:50 - 1:200 Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 120-340 of human CCT6B (NP_006575.2). Synonyms CCT6B;CCT-zeta-2;CCTZ-2;Cctz2;TCP-1-zeta-2;TSA303 Contact Product Information www.abclonal.com Source Isotype Purification Rabbit IgG Affinity purification Storage Store at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3. Validation Data Western blot analysis of extracts of various cell lines, using CCT6B antibody (A14615) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit (RM00020). Exposure time: 15s. Immunofluorescence analysis of HeLa cells Immunofluorescence analysis of L929 cells using CCT6B antibody (A14615) at dilution using CCT6B antibody (A14615) at dilution of 1:100. Blue: DAPI for nuclear staining. of 1:100. Blue: DAPI for nuclear staining. Antibody | Protein | ELISA Kits | Enzyme | NGS | Service For research use only. Not for therapeutic or diagnostic purposes. Please visit http://abclonal.com for a complete listing of recommended products..

Copy Link

Recommended publications

Genome-Wide Analysis Reveals Selection Signatures Involved in Meat Traits and Local Adaptation in Semi-Feral Maremmana Cattle
Genome-Wide Analysis Reveals Selection Signatures Involved in Meat Traits and Local Adaptation in Semi-Feral Maremmana Cattle Slim Ben-Jemaa, Gabriele Senczuk, Elena Ciani, Roberta Ciampolini, Gennaro Catillo, Mekki Boussaha, Fabio Pilla, Baldassare Portolano, Salvatore Mastrangelo To cite this version: Slim Ben-Jemaa, Gabriele Senczuk, Elena Ciani, Roberta Ciampolini, Gennaro Catillo, et al.. Genome-Wide Analysis Reveals Selection Signatures Involved in Meat Traits and Local Adaptation in Semi-Feral Maremmana Cattle. Frontiers in Genetics, Frontiers, 2021, 10.3389/fgene.2021.675569. hal-03210766 HAL Id: hal-03210766 https://hal.inrae.fr/hal-03210766 Submitted on 28 Apr 2021 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Distributed under a Creative Commons Attribution| 4.0 International License ORIGINAL RESEARCH published: 28 April 2021 doi: 10.3389/fgene.2021.675569 Genome-Wide Analysis Reveals Selection Signatures Involved in Meat Traits and Local Adaptation in Semi-Feral Maremmana Cattle Slim Ben-Jemaa 1, Gabriele Senczuk 2, Elena Ciani 3, Roberta
[Show full text]
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Page 1 of 781 Diabetes A Computational Approach for Defining a Signature of β-Cell Golgi Stress in Diabetes Mellitus Robert N. Bone1,6,7, Olufunmilola Oyebamiji2, Sayali Talware2, Sharmila Selvaraj2, Preethi Krishnan3,6, Farooq Syed1,6,7, Huanmei Wu2, Carmella Evans-Molina 1,3,4,5,6,7,8* Departments of 1Pediatrics, 3Medicine, 4Anatomy, Cell Biology & Physiology, 5Biochemistry & Molecular Biology, the 6Center for Diabetes & Metabolic Diseases, and the 7Herman B. Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis, IN 46202; 2Department of BioHealth Informatics, Indiana University-Purdue University Indianapolis, Indianapolis, IN, 46202; 8Roudebush VA Medical Center, Indianapolis, IN 46202. *Corresponding Author(s): Carmella Evans-Molina, MD, PhD ([email protected]) Indiana University School of Medicine, 635 Barnhill Drive, MS 2031A, Indianapolis, IN 46202, Telephone: (317) 274-4145, Fax (317) 274-4107 Running Title: Golgi Stress Response in Diabetes Word Count: 4358 Number of Figures: 6 Keywords: Golgi apparatus stress, Islets, β cell, Type 1 diabetes, Type 2 diabetes 1 Diabetes Publish Ahead of Print, published online August 20, 2020 Diabetes Page 2 of 781 ABSTRACT The Golgi apparatus (GA) is an important site of insulin processing and granule maturation, but whether GA organelle dysfunction and GA stress are present in the diabetic β-cell has not been tested. We utilized an informatics-based approach to develop a transcriptional signature of β-cell GA stress using existing RNA sequencing and microarray datasets generated using human islets from donors with diabetes and islets where type 1(T1D) and type 2 diabetes (T2D) had been modeled ex vivo. To narrow our results to GA-specific genes, we applied a filter set of 1,030 genes accepted as GA associated.
[Show full text]
Sequence Composition and Evolution of Mammalian B Chromosomes
G C A T T A C G G C A T genes Review Sequence Composition and Evolution of Mammalian B Chromosomes Nikolay B. Rubtsov 1,2,* and Yury M. Borisov 3 1 The Federal Research Center Institute of Cytology and Genetics SB RAS, Lavrentiev Ave. 10, Novosibirsk 630090, Russia 2 Novosibirsk State University, Pirogova Str. 2, Novosibirsk 630090, Russia 3 Severtzov Institute of Ecology and Evolution, Russia Academy of Sciences, Leninsky Pr. 33, Moscow 119071, Russia; [email protected] * Correspondence: [email protected]; Tel.: +7-913-941-5682 Received: 28 August 2018; Accepted: 1 October 2018; Published: 10 October 2018 Abstract: B chromosomes (Bs) revealed more than a hundred years ago remain to be some of the most mysterious elements of the eukaryotic genome. Their origin and evolution, DNA composition, transcriptional activity, impact on adaptiveness, behavior in meiosis, and transfer to the next generation require intensive investigations using modern methods. Over the past years, new experimental techniques have been applied and helped us gain a deeper insight into the nature of Bs. Here, we consider mammalian Bs, taking into account data on their DNA sequencing, transcriptional activity, positions in nuclei of somatic and meiotic cells, and impact on genome functioning. Comparative cytogenetics of Bs suggests the existence of different mechanisms of their formation and evolution. Due to the long and complicated evolvement of Bs, the similarity of their morphology could be explained by the similar mechanisms involved in their development while the difference between Bs even of the same origin could appear due to their positioning at different stages of their evolution.
[Show full text]
THE GENETIC ARCHITECTURE of the DDK SYNDROME: an EARLY EMBRYONIC LETHAL PHENOTYPE in the MOUSE Folami Yetunde Ideraabdullah a Di
THE GENETIC ARCHITECTURE OF THE DDK SYNDROME: AN EARLY EMBRYONIC LETHAL PHENOTYPE IN THE MOUSE Folami Yetunde Ideraabdullah A dissertation submitted to the faculty of the University of North Carolina at Chapel Hill in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Curriculum in Genetics and Molecular Biology. Chapel Hill 2007 Approved by: Fernando Pardo-Manuel de Villena, PhD Scott Bultman, PhD Beverly Koller, PhD Karen Mohlke, PhD David Threadgill, PhD ABSTRACT Folami Yetunde Ideraabdullah: The Genetic Architecture of the DDK Syndrome: An Early Embryonic Lethal Phenotype in the Mouse (Under the direction of Fernando Pardo-Manuel de Villena) The DDK syndrome is a polar early embryonic lethal phenotype that occurs when DDK females are mated to males of other inbred mouse strains. Lethality is parent of origin dependent and results from an incompatibility between an ooplasmic DDK factor and a non- DDK paternal gene, both of which map to the Ovum mutant (Om) locus on chromosome 11. Here, I utilize naturally occurring genetic variation in classical and wild-derived inbred strains to characterize the genetic architecture of the DDK syndrome. I show that genetic variation among wild-derived strains is uniformly distributed and significantly higher than previously reported for other mammalian species. The high levels of diversity present among laboratory strains suggests that the effective population size of the Mus lineage has been relatively large and constant over a long period of time. Overall, these findings demonstrate that wild- derived inbred strains are a valuable resource for genetic studies. By utilizing this resource in recombination mapping and association mapping experiments, we have reduced the candidate interval for the paternal gene of the DDK syndrome to a 23 kb region encompassing a single gene.
[Show full text]
Human Induced Pluripotent Stem Cell–Derived Podocytes Mature Into Vascularized Glomeruli Upon Experimental Transplantation
BASIC RESEARCH www.jasn.org Human Induced Pluripotent Stem Cell–Derived Podocytes Mature into Vascularized Glomeruli upon Experimental Transplantation † Sazia Sharmin,* Atsuhiro Taguchi,* Yusuke Kaku,* Yasuhiro Yoshimura,* Tomoko Ohmori,* ‡ † ‡ Tetsushi Sakuma, Masashi Mukoyama, Takashi Yamamoto, Hidetake Kurihara,§ and | Ryuichi Nishinakamura* *Department of Kidney Development, Institute of Molecular Embryology and Genetics, and †Department of Nephrology, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan; ‡Department of Mathematical and Life Sciences, Graduate School of Science, Hiroshima University, Hiroshima, Japan; §Division of Anatomy, Juntendo University School of Medicine, Tokyo, Japan; and |Japan Science and Technology Agency, CREST, Kumamoto, Japan ABSTRACT Glomerular podocytes express proteins, such as nephrin, that constitute the slit diaphragm, thereby contributing to the ﬁltration process in the kidney. Glomerular development has been analyzed mainly in mice, whereas analysis of human kidney development has been minimal because of limited access to embryonic kidneys. We previously reported the induction of three-dimensional primordial glomeruli from human induced pluripotent stem (iPS) cells. Here, using transcription activator–like effector nuclease-mediated homologous recombination, we generated human iPS cell lines that express green ﬂuorescent protein (GFP) in the NPHS1 locus, which encodes nephrin, and we show that GFP expression facilitated accurate visualization of nephrin-positive podocyte formation in
[Show full text]
Primepcr™Assay Validation Report
PrimePCR™Assay Validation Report Gene Information Gene Name chaperonin containing TCP1, subunit 6B (zeta 2) Gene Symbol CCT6B Organism Human Gene Summary This gene encodes a molecular chaperone that is a member of the chaperonin containing TCP1 complex (CCT) also known as the TCP1 ring complex (TRiC). This complex consists of two identical stacked rings each containing eight different proteins. Unfolded polypeptides enter the central cavity of the complex and are folded in an ATP-dependent manner. The complex folds various proteins including actin and tubulin. Alternate transcriptional splice variants encoding different isoforms have been found for this gene. Gene Aliases CCT-zeta-2, CCTZ-2, Cctz2, TCP-1-zeta-2, TSA303 RefSeq Accession No. NC_000017.10, NT_010799.15 UniGene ID Hs.73072 Ensembl Gene ID ENSG00000132141 Entrez Gene ID 10693 Assay Information Unique Assay ID qHsaCID0017299 Assay Type SYBR® Green Detected Coding Transcript(s) ENST00000421975, ENST00000314144, ENST00000436961 Amplicon Context Sequence TCCTAATTTATGCTTCATCTCCATTATTTCTACCATGAAGAGATCAATAGGGTAAC CTGGTCTTCTAACAGCCAAAACAGAATCCACCACAACCTCTGTTAAGACATCAGC CAGTTCAGCATGAACTTTAGTTTGTAATGATGTTCTAGCTACATCTAAGAGGATT Amplicon Length (bp) 136 Chromosome Location 17:33278980-33281517 Assay Design Intron-spanning Purification Desalted Validation Results Efficiency (%) 97 R2 0.9991 cDNA Cq 24.89 cDNA Tm (Celsius) 80.5 Page 1/5 PrimePCR™Assay Validation Report gDNA Cq Specificity (%) 100 Information to assist with data interpretation is provided at the end of this report. Page 2/5
[Show full text]
Prognostic and Functional Significant of Heat Shock Proteins (Hsps)
biology Article Prognostic and Functional Significant of Heat Shock Proteins (HSPs) in Breast Cancer Unveiled by Multi-Omics Approaches Miriam Buttacavoli 1,†, Gianluca Di Cara 1,†, Cesare D’Amico 1, Fabiana Geraci 1 , Ida Pucci-Minafra 2, Salvatore Feo 1 and Patrizia Cancemi 1,2,* 1 Department of Biological Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, 90128 Palermo, Italy; [email protected] (M.B.); [email protected] (G.D.C.); [email protected] (C.D.); [email protected] (F.G.); [email protected] (S.F.) 2 Experimental Center of Onco Biology (COBS), 90145 Palermo, Italy; [email protected] * Correspondence: [email protected]; Tel.: +39-091-2389-7330 † These authors contributed equally to this work. Simple Summary: In this study, we investigated the expression pattern and prognostic significance of the heat shock proteins (HSPs) family members in breast cancer (BC) by using several bioinfor- matics tools and proteomics investigations. Our results demonstrated that, collectively, HSPs were deregulated in BC, acting as both oncogene and onco-suppressor genes. In particular, two different HSP-clusters were significantly associated with a poor or good prognosis. Interestingly, the HSPs deregulation impacted gene expression and miRNAs regulation that, in turn, affected important bio- logical pathways involved in cell cycle, DNA replication, and receptors-mediated signaling. Finally, the proteomic identification of several HSPs members and isoforms revealed much more complexity Citation: Buttacavoli, M.; Di Cara, of HSPs roles in BC and showed that their expression is quite variable among patients. In conclusion, G.; D’Amico, C.; Geraci, F.; we elaborated two panels of HSPs that could be further explored as potential biomarkers for BC Pucci-Minafra, I.; Feo, S.; Cancemi, P.
[Show full text]
Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
bioRxiv preprint doi: https://doi.org/10.1101/083428; this version posted April 3, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Title Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder Author List Deidre R. Krupp,1,6 Rebecca A. Barnard,1,6 Yannis Duffourd,2 Sara A. Evans,1 Ryan M. Mulqueen,1 Raphael Bernier,3 Jean-Baptiste Rivière,4 Eric Fombonne,5 and Brian J. O’Roak1,* Affiliations 1Department of Molecular & Medical Genetics, Oregon Health & Science University, Portland, OR 97239, USA; 2Equipe d’Accueil 4271, Génétique des Anomalies du Développement, Université Bourgogne Franche-Comté, 21000 Dijon, France; 3Department of Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, 98195 USA; 4Deparmtent of Human Genetics, McGill University, Montréal, QC H3A 1B1, Canada; 5Deparment of Psychiatry, Oregon Health & Science University, Portland, OR 97239, USA 6These authors contributed equally to this work *Correspondence: [email protected], @TheRealDrOLab 1 bioRxiv preprint doi: https://doi.org/10.1101/083428; this version posted April 3, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Abstract Genetic risk factors for autism spectrum disorder (ASD) have yet to be fully elucidated. Postzygotic mosaic mutations (PMMs) have been implicated in several neurodevelopmental disorders and overgrowth syndromes. We systematically evaluated PMMs by leveraging whole- exome sequencing data on a large family-based ASD cohort, the Simons Simplex Collection. We found evidence that 11% of published single nucleotide variant (SNV) de novo mutations are potentially PMMs.
[Show full text]
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham a Thesis Submitted in Conformity
Characterizing Genomic Duplication in Autism Spectrum Disorder by Edward James Higginbotham A thesis submitted in conformity with the requirements for the degree of Master of Science Graduate Department of Molecular Genetics University of Toronto © Copyright by Edward James Higginbotham 2020 i Abstract Characterizing Genomic Duplication in Autism Spectrum Disorder Edward James Higginbotham Master of Science Graduate Department of Molecular Genetics University of Toronto 2020 Duplication, the gain of additional copies of genomic material relative to its ancestral diploid state is yet to achieve full appreciation for its role in human traits and disease. Challenges include accurately genotyping, annotating, and characterizing the properties of duplications, and resolving duplication mechanisms. Whole genome sequencing, in principle, should enable accurate detection of duplications in a single experiment. This thesis makes use of the technology to catalogue disease relevant duplications in the genomes of 2,739 individuals with Autism Spectrum Disorder (ASD) who enrolled in the Autism Speaks MSSNG Project. Fine-mapping the breakpoint junctions of 259 ASD-relevant duplications identified 34 (13.1%) variants with complex genomic structures as well as tandem (193/259, 74.5%) and NAHR- mediated (6/259, 2.3%) duplications. As whole genome sequencing-based studies expand in scale and reach, a continued focus on generating high-quality, standardized duplication data will be prerequisite to addressing their associated biological mechanisms. ii Acknowledgements I thank Dr. Stephen Scherer for his leadership par excellence, his generosity, and for giving me a chance. I am grateful for his investment and the opportunities afforded me, from which I have learned and benefited. I would next thank Drs.
[Show full text]
The Landscape of Molecular Chaperones Across Human Tissues Reveals a Layered Architecture of Core and Variable Chaperones
bioRxiv preprint doi: https://doi.org/10.1101/2020.03.04.976720; this version posted March 5, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. The landscape of molecular chaperones across human tissues reveals a layered architecture of core and variable chaperones Netta Shemesh1,2+, Juman Jubran1+, Mehtap Abu-Qarn2, Eyal Simonovky1, Omer Basha1, Idan Hekselman1, Shiran Dror2, Ekaterina Vinogradov1, Serena Carra3, Anat Ben-Zvi2* and Esti Yeger-Lotem1* 1 Department of Clinical Biochemistry and Pharmacology and the National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel 2 Department of Life Sciences, Ben-Gurion University of the Negev, Beer Sheva 84105, Israel 3 Centre for Neuroscience and Nanotechnology, Department of Biomedical, Metabolic and Neural Sciences, University of Modena and Reggio Emilia, Modena, Italy + These authors contributed equally to this study. * Correspondence to: Prof. Esti Yeger-Lotem, Email: [email protected] Prof. Anat Ben-Zvi, Email: [email protected] 1 bioRxiv preprint doi: https://doi.org/10.1101/2020.03.04.976720; this version posted March 5, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY 4.0 International license. Abstract The sensitivity of the protein-folding environment to chaperone disruption can be highly tissue-specific.
[Show full text]
Multiple Splice Variants of Lactate Dehydrogenase C Selectively Expressed in Human Cancer1, 2
[CANCER RESEARCH 62, 6750–6755, November 15, 2002] Multiple Splice Variants of Lactate Dehydrogenase C Selectively Expressed in Human Cancer1, 2 Michael Koslowski, O¨ zlem Tu¨reci, Carolin Bell, Patricia Krause, Hans-Anton Lehr, Joachim Brunner, Gerhard Seitz, Frank Oliver Nestle, Christoph Huber, and Ugur Sahin3 Department of Internal Medicine, University Mainz, 55131 Mainz, Germany [M. K., O¨ . T., C. B., P. K., C. H., U. S.]; Institute of Pathology, University Mainz, 55131 Mainz, Germany [H-A. L., J. B.]; Institute of Pathology, Clinical Center Bamberg, 96049 Bamberg, Germany [G. S.]; and Department of Dermatology, University Hospital Zuerich, 8091 Zuerich, Switzerland [F. O. N.] ABSTRACT individual CT genes are expressed in only 20–40% of most tumor types, a polyvalent CT vaccine strategy would be an effective way to We applied a combined data mining and experimental validation ap- increase the number of cancer patients eligible for vaccination and proach for the discovery of germ cell-specific genes aberrantly expressed additional tumor antigens need to be defined. To identify tumor in cancer. Six of 21 genes with confirmed germ cell specificity were detected in tumors, indicating that ectopic activation of testis-specific antigens beyond those isolated on the basis of their immunogenicity, genes in cancer is a frequent phenomenon. Most surprisingly one of the representational difference analysis was successfully adopted (14– genes represented lactate dehydrogenase C (LDHC), the germ cell-specific 16). As reported here, we used a combined strategy based on data member of the lactate dehydrogenase family. LDHC escapes from tran- mining and subsequent experimental validation to identify additional scriptional repression, resulting in significant expression levels in virtually germ cell-specific genes activated in cancer.
[Show full text]
CCT6B Purified Maxpab Rabbit Polyclonal Antibody (D01P)
CCT6B purified MaxPab rabbit polyclonal antibody (D01P) Catalog # : H00010693-D01P 規格 : [ 100 ug ] List All Specification Application Image Product Rabbit polyclonal antibody raised against a full-length human CCT6B Western Blot (Transfected lysate) Description: protein. Immunogen: CCT6B (AAH27591.1, 1 a.a. ~ 530 a.a) full-length human protein. Sequence: MAAIKAVNSKAEVARAQAALAVNICAARGLQDVLRTNLGPKGTMKMLAS GAGDIKLTKDGNVLLDEMQIQHPTASLIAKVATAQDDVTGDGTTSNVLIIG ELLKQADLYISEGLHPRIIAEGFEAAKIKALEVLEEVKVTKEMKRKILLDVAR enlarge TSLQTKVHAELADVLTEVVVDSVLAVRRPGYPIDLFMVEIMEMKHKLGTD TKLIQGLVLDHGARHPDMKKRVEDAFILICNVSLEYEKTEVNSGFFYKTAE EKEKLVKAERKFIEDRVQKIIDLKDKVCAQSNKGFVVINQKGIDPFSLDSLA KHGIVALRRAKRRNMERLSLACGGMAVNSFEDLTVDCLGHAGLVYEYTL GEEKFTFIEECVNPCSVTLLVKGPNKHTLTQVKDAIRDGLRAIKNAIEDGC MVPGAGAIEVAMAEALVTYKNSIKGRARLGVQAFADALLIIPKVLAQNAGY DPQETLVKVQAEHVESKQLVGVDLNTGEPMVAADAGVWDNYCVKKQLL HSCTVIATNILLVDEIMRAGMSSLK Host: Rabbit Reactivity: Human Quality Control Antibody reactive against mammalian transfected lysate. Testing: Storage Buffer: In 1x PBS, pH 7.4 Storage Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. Instruction: MSDS: Download Datasheet: Download Applications Western Blot (Transfected lysate) Western Blot analysis of CCT6B expression in transfected 293T cell line (H00010693-T02) by CCT6B MaxPab polyclonal antibody. Lane 1: CCT6B transfected lysate(57.80 KDa). Page 1 of 2 2016/5/23 Lane 2: Non-transfected lysate. Protocol Download Gene Information Entrez GeneID: 10693 GeneBank BC027591.1 Accession#: Protein AAH27591.1 Accession#:
[Show full text]