TissueScan, Human Brain cDNA Array

CAT＃: HBRT101

24 samples covering all major human brain normal tissues at different locations. Available in 2, 5, 10 identical plates.

Size: 2 Panels 5 Panels 10 Panels

Datasheet
SDS

CNY 4,560.00

货期*
5周
规格
    • 2 Panels
Cited in 41 publications.

Product images

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Specifications

Product Data
Array Category Normal Tissue
Clinical Info N/A
Tissue Brain
Array Name Human Brain cDNA Array
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Citations (41)

The use of this Tissues has been cited in the following citations:
Calsyntenin-3 interacts with the sodium-dependent vitamin C transporter-2 to regulate vitamin C uptake ,null, International journal of biological macromolecules ,PubMed ID 34673103
FIBCD1 is an endocytic GAG receptor associated with a novel neurodevelopmental disorder. ,null, EMBO molecular medicine ,PubMed ID 35916241
Nitric-Oxide Synthase trafficking inducer (NOSTRIN) is an emerging negative regulator of colon cancer progression ,null, BMC Cancer ,PubMed ID 35642021
Genome-wide in vivo CNS Screening Identifies Genes that Modify CNS Neuronal Survival and mHTT Toxicity ,null, Neuron ,PubMed ID 32004439
Small mitochondrial protein NERCLIN regulates cardiolipin homeostasis and mitochondrial ultrastructure ,Konovalova, S;Torregrosa-Muñumer, R;Manjunath, P;Baral, S;Liu, X;Holopainen, M;Kvist, J;Rajendran, J;Yang, Y;Varjosalo, M;Käkelä, R;Somerharju, P;Tyynismaa, H;, bioRxiv [Human Brain]
Mutations in FAM50A suggest that Armfield XLID syndrome is a spliceosomopathy ,Lee, YR;Khan, K;Armfield-Uhas, K;Srikanth, S;Thompson, NA;Pardo, M;Yu, L;Norris, JW;Peng, Y;Gripp, KW;Aleck, KA;Li, C;Spence, E;Choi, TI;Kwon, SJ;Park, HM;Yu, D;Do Heo, W;Mooney, MR;Baig, SM;Wentzensen, IM;Telegrafi, A;McWalter, K;Moreland, T;Roadhouse, C;Ramsey, K;Lyons, MJ;Skinner, C;Alexov, E;Katsanis, N;Stevenson, RE;Choudhary, JS;Adams, DJ;Kim, CH;Davis, EE;Schwartz, CE;, Nat Commun ,PubMed ID 32703943 [Human Brain]
CYP17A1 deficient XY mice display susceptibility to atherosclerosis, altered lipidomic profile and atypical sex development ,null, Scientific Reports ,PubMed ID 32472014
FAM19A1, a brain-enriched and metabolically responsive neurokine, regulates food intake patterns and mouse behaviors ,Lei, X;Liu, L;Terrillion, CE;Karuppagounder, SS;Cisternas, P;Lay, M;Martinelli, DC;Aja, S;Dong, X;Pletnikov, MV;Wong, GW;, FASEB J. ,PubMed ID 31689372 [Human Brain]
A novel histone H4 variant H4G regulates rDNA transcription in breast cancer ,null, Nucleic Acids Research ,PubMed ID 31219579
FOCAD loss impacts microtubule assembly, G2/M progression and patient survival in astrocytic gliomas. ,null, Acta neuropathologica ,PubMed ID 31473790
Genetic Polymorphisms within The Intronless ACTL7A andACTL7B Genes Encoding Spermatogenesis-Specific Actin-Like Proteins in Japanese Males ,null, International Journal of Fertility & Sterility ,PubMed ID 31310081
Widespread Accumulation of Ribosome-Associated Isolated 3′ UTRs in Neuronal Cell Populations of the Aging Brain ,Sudmant, PH;Lee, H;Dominguez, D;Heiman, M;, Cell Reports ,PubMed ID 30485811 [Human Brain]
Relevance of polymorphisms in MC4R and BDNF in short normal stature ,Herrfurth, N;Volckmar, AL;Peters, T;Kleinau, G;Müller, A;Cetindag, C;Schonnop, L;Föcker, M;Dempfle, A;Wudy, SA;Grant, SFA;Reinehr, T;Cousminer, DL;Hebebrand, J;Biebermann, H;Hinney, A;, BMC Pediatr ,PubMed ID 30134862 [Human Brain]
Integrated Systems Biology Approach Identifies Novel Maternal and Placental Pathways of Preeclampsia ,null, Frontiers in Immunology ,PubMed ID 30135684
CRISPR whole-genome screening identifies new necroptosis regulators and RIPK1 alternative splicing ,Callow, MG;Watanabe, C;Wickliffe, KE;Bainer, R;Kummerfield, S;Weng, J;Cuellar, T;Janakiraman, V;Chen, H;Chih, B;Liang, Y;Haley, B;Newton, K;Costa, MR;, Cell Death Dis ,PubMed ID 29449584 [Human Brain]
Early Life Allergen and Air Pollutant Exposures Alter Longitudinal Blood Immune Profiles in Infant Rhesus Monkeys ,null, Toxicology and applied pharmacology ,PubMed ID 28529118
Nogo-B receptor deficiency increases LXRα nuclear translocation and hepatic lipogenesis via an AMPKα-dependent pathway ,null, Hepatology (Baltimore, Md.) ,PubMed ID 27480224
A thrifty variant in CREBRF strongly influences body mass index in Samoans ,Minster, RL;Hawley, NL;Su, CT;Sun, G;Kershaw, EE;Cheng, H;Buhule, OD;Lin, J;Reupena, MS;Viali, S;Tuitele, J;Naseri, T;Urban, Z;Deka, R;Weeks, DE;McGarvey, ST;, Nat. Genet. ,PubMed ID 27455349
Multi-species sequence comparison reveals conservation of ghrelin gene-derived splice variants encoding a truncated ghrelin peptide ,null, Endocrine ,PubMed ID 26792793
ZC4H2, an XLID gene, is required for the generation of a specific subset of CNS interneurons ,May, M;Hwang, KS;Miles, J;Williams, C;Niranjan, T;Kahler, SG;Chiurazzi, P;Steindl, K;Van Der Spek, PJ;Swagemakers, S;Mueller, J;Stefl, S;Alexov, E;Ryu, JI;Choi, JH;Kim, HT;Tarpey, P;Neri, G;Holloway, L;Skinner, C;Stevenson, RE;Dorsky, RI;Wang, T;Schwartz,, Hum. Mol. Genet. ,PubMed ID 26056227 [HBRT101]
Regulation of SPRY3 by X chromosome and PAR2-linked promoters in an autism susceptibility region ,Ning, Z;McLellan, AS;Ball, M;Wynne, F;O'Neill, C;Mills, W;Quinn, JP;Kleinjan, DA;Anney, RJ;Carmody, RJ;O'Keeffe, G;Moore, T;, Hum. Mol. Genet. ,PubMed ID 26089202 [HBRT101]
Progranulin Transcripts with Short and Long 5′ Untranslated Regions (UTRs) Are Differentially Expressed via Posttranscriptional and Translational Repression * ,null, The Journal of Biological Chemistry ,PubMed ID 25056957
Distribution of insulin mRNA transcripts within the human body ,Bell, GD;Reddy, S;Sun, X;Yang, Y;Krissansen, GW;, Biochem. Biophys. Res. Commun. ,PubMed ID 25110147 [PS100033]
β3-Chimaerin, a novel member of the chimaerin Rac-GAP family ,Zubeldia-Brenner, L;Gutierrez-Uzquiza, A;Barrio-Real, L;Wang, H;Kazanietz, MG;Leskow, FC;, Mol. Biol. Rep., Jan 2014. ,PubMed ID 24430297 [Human Brain Panel I]
C1q/TNF-related protein 4 (CTRP4) is a unique secreted protein with two tandem C1q domains that functions in the hypothalamus to modulate food intake and body weight ,Byerly, MS;Petersen, PS;Ramamurthy, S;Seldin, MM;Lei, X;Provost, E;Wei, Z;Ronnett, GV;Wong, GW;, J. Biol. Chem. Dec 2013. ,PubMed ID 24366864 [human brain normal tissue panel]
Elucidating Novel Hepatitis C Virus–Host Interactions Using Combined Mass Spectrometry and Functional Genomics Approaches * ,null, Molecular & Cellular Proteomics : MCP ,PubMed ID 24169621
Chemerin is expressed mainly in pancreas and liver, is regulated by energy deprivation and lacks day/night variation in humans ,null, European journal of endocrinology / European Federation of Endocrine Societies ,PubMed ID 23904282
Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma ,null, Nature genetics ,PubMed ID 23064416
Ectopic lymphoid tissue alters the chemokine gradient, increases lymphocyte retention and exacerbates murine ileitis ,null, Gut ,PubMed ID 22267601
Pigment Epithelium-Derived Factor (PEDF) Interacts with Transportin SR2, and Active Nuclear Import Is Facilitated by a Novel Nuclear Localization Motif ,null, PLoS ONE ,PubMed ID 22028839
Phosphatidylinositol 4-phosphate 5-kinase I?_v6, a new splice variant found in rodents and humans ,null, Biochemical and Biophysical Research Communications ,PubMed ID 21756881
Pleiomorphic Adenoma Gene-like 2 Expression Is Associated with the Development of Lung Adenocarcinoma and Emphysema ,null, Lung cancer (Amsterdam, Netherlands) ,PubMed ID 21397355
hHSS1: a novel secreted factor and suppressor of glioma growth located at chromosome 19q13.33 ,null, Journal of Neuro-Oncology ,PubMed ID 20680400
Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome ,null, American Journal of Human Genetics ,PubMed ID 19026396
Hepatocyte nuclear factor 4? in the intestinal epithelial cells protects against inflammatory bowel disease ,null, ,PubMed ID 18338782
Identification of functional type 1 ryanodine receptors in human dendritic cells ,null, Biochemical and Biophysical Research Communications ,PubMed ID 17707769
Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts ,null, BMC Genomics ,PubMed ID 17727735
Tau and saitohin gene expression pattern in progressive supranuclear palsy ,null, Brain Research ,PubMed ID 17320831
Increased large conductance calcium-activated potassium (BK) channel expression accompanied by STREX variant downregulation in the developing mouse CNS ,null, BMC Developmental Biology ,PubMed ID 16872513
Increased Expression in Dorsolateral Prefrontal Cortex of CAPON in Schizophrenia and Bipolar DisorderCAPON and Schizophrenia--Does Size Matter?Does the CAPON Gene Confer Susceptibility for Schizophrenia? ,null, PLoS Medicine ,PubMed ID 16146415
Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality ,null, Proceedings of the National Academy of Sciences of the United States of America ,PubMed ID 15383666
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