Higd1c

WebGene_name: HIGD1C UBIE UBIE2 Protein_name: HIG1C Humangene_id : 613227 Humanswissprot _no: A8MV81 Mousegene_id:380975 Mouseswissprot _no: Q76I25 Immunogen: Synthesized peptide derived from human HIG1C Specificity: This antibody detects endogenous levels of HIG1C at Human/Mouse Web21 de mar. de 2024 · MTERF3 (Mitochondrial Transcription Termination Factor 3) is a Protein Coding gene. Diseases associated with MTERF3 include Spastic Paraplegia 7, Autosomal Recessive.Among its related pathways are Selective autophagy and Mitophagy.Gene Ontology (GO) annotations related to this gene include transcription cis …

NM_001109619.4(HIGD1C):c.191T>C (p.Val64Ala) AND Inborn …

WebDownload scientific diagram Hypoxia-inducible Higd1a directly binds to highly purified cytochrome c oxidase (hpCcO). ( A ) Heat map of three genes ( Upper ) identified as … WebOriGene higd1c myc flag in pcmv6 entry mouse Higd1c Myc Flag In Pcmv6 Entry Mouse, supplied by OriGene, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more how to replace a schlage door knob https://pattyindustry.com

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Web上海康朗生物科技有限公司主要致力于“Anti-HIGD1C抗体”的生产销售。多年的“Anti-HIGD1C抗体”生产与销售的经验,与各行业新老用户建立了稳定的合作关系,我公司经营的产品名称深受广大用户信赖。欢迎来电咨询或前来选购。 联系电话:021-61998208。 Web21 de mar. de 2024 · Entrez Gene Summary for HIGD2A Gene. The protein encoded by this gene is a subunit of the cytochrome c oxidase complex (complex IV), which is the … WebHIGD1C-001: 371: 97aa: ENSP00000381473.3 . Gene/transcipt that contains an open reading frame (ORF). Protein coding. CCDS44882: A8MV81: NM_001109619.1: The … north aot

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Higd1c

Tissue-specific mitochondrial HIGD1C promotes oxygen sensitivity …

WebHIGD1C (Q18059289) From Wikidata. Jump to navigation Jump to search. protein-coding gene in the species Homo sapiens. GM921; HIG1 hypoxia inducible domain family member 1C; edit. Language Label Description Also known as; English: HIGD1C. protein-coding gene in the species Homo sapiens. GM921; HIG1 hypoxia inducible domain family member 1C; Web1 de jul. de 2008 · Protein. HIG1 domain family member 1C. Gene. HIGD1C. Status. UniProtKB reviewed (Swiss-Prot) Organism. Homo sapiens (Human) Amino acids.

Higd1c

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WebHIGD1C (Q18059289) From Wikidata. Jump to navigation Jump to search. protein-coding gene in the species Homo sapiens. GM921; HIG1 hypoxia inducible domain family … WebThe hypothalamus is a part of the diencephalon, together with the thalamus, epithalamus, subthalamus and meta-thalamus. The hypothalamus develops from the embryonic diencephalon and is located at the bottom of the diencephalon. In humans, it is an almond-like structure. The hypothalamus is the center of the vegetative nervous system as well …

Web1 de nov. de 2014 · HIGD1C (HIG1 hypoxia inducible domain family member 1C) 2014-11-01 Affiliation Identity. HGNC. HIGD1C. LOCATION. 12q13.12. LOCUSID. 613227. … Web21 de mar. de 2024 · GeneCards Summary for HIGD1C Gene. HIGD1C (HIG1 Hypoxia Inducible Domain Family Member 1C) is a Protein Coding gene. Diseases associated …

Web丁香通为您提供抗小鼠CD31单克隆抗体商品详情介绍:价格:¥11,货号:RD21985F,品牌:Reddot Biotech,产地:加拿大,详见丁香通抗小鼠CD31单克隆抗体商品详情页; WebSostanze chimiche e Farmaci 127. Fattori Di Trascrizione Argonaute Proteins Piccoli Rna Di Interferenza Eterocromatina Proteine Dell'Arabidopsis Simporti Idrogeno-Fosfato Rna Delle Piante Rna Antisenso Proteine Nucleari Rna Messaggero Cromatina Proteine Leganti Dna Istoni Fattore Di Trascrizione Sp1 Rna A Doppia Elica Dna Delle Piante Rna Non …

Web21 de mar. de 2024 · TRPM8 (Transient Receptor Potential Cation Channel Subfamily M Member 8) is a Protein Coding gene. Diseases associated with TRPM8 include Migraine Without Aura and Photokeratitis.Among its related pathways are Ion channel transport and CREB Pathway.Gene Ontology (GO) annotations related to this gene include protein …

WebHIGD1C HIG1 hypoxia inducible domain family member 1C [ (green monkey)] Gene ID: 103238311, updated on 16-Aug-2024. Summary Other designations. HIG1 domain family member 1C northaphid9Web胎牛血清(杂交瘤细胞专用) sp2/0 小鼠骨髓瘤细胞. 佐剂乳化器 how to replace a seat disk toilet flapperWebNM_001109619.4(HIGD1C):c.191T>C (p.Val64Ala) AND Inborn genetic diseases Clinical significance: Uncertain significance (Last evaluated: Apr 22, 2024) Review status: 1 star out of maximum of 4 stars how to replace a sata hard driveWebHIGD1C (Gm921) protein expression summary. We use cookies to enhance the usability of our website. If you continue, we'll assume that you are happy to receive all cookies. More information. Don't show this again. HIGD1C. SECTIONS. TISSUE BRAIN SINGLE CELL TYPE TISSUE CELL TYPE PATHOLOGY DISEASE north apennines wwiiWebASSOCIATED WITH genetic disease (ortholog); FOUND IN membrane (inferred); INTERACTS WITH 2,3',4,4',5-Pentachlorobiphenyl (ortholog); 2,3,7,8 … northapartments chemnitzWebImmunoglobulins, also known as antibodies, are membrane-bound or secreted glycoproteins produced by B lymphocytes. In the recognition phase of humoral immunity, the … how to replace a schlage lock cylinderWeb1 de nov. de 2014 · HIGD1C (HIG1 hypoxia inducible domain family member 1C) 2014-11-01 Affiliation Identity. HGNC. HIGD1C. LOCATION. 12q13.12. LOCUSID. 613227. ALIAS. GM921. Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool. northaparthotel bucharest