GFAP (NM_002055) Human Untagged Clone

SKU
SC118873
GFAP (untagged)-Human glial fibrillary acidic protein (GFAP), transcript variant 1
  $457.00
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Specifications
Specifications
Product Data
Type Human Untagged Clone
Target Symbol GFAP
Synonyms ALXDRD
Vector pCMV6-XL4
E. coli Selection Ampicillin (100 ug/mL)
Mammalian Cell Selection None
Sequence Data
Fully Sequenced ORF
>OriGene ORF within SC118873 sequence for NM_002055 edited (data generated by NextGen Sequencing)
ATGGAGAGGAGACGCATCACCTCCGCTGCTCGCCGCTCCTACGTCTCCTCAGGGGAGATG
ATGGTGGGGGGCCTGGCTCCTGGCCGCCGTCTGGGTCCTGGCACCCGCCTCTCCCTGGCT
CGAATGCCCCCTCCACTCCCAACCCGGGTGGATTTCTCCCTGGCTGGGGCACTCAATGCT
GGCTTCAAGGAGACCCGGGCCAGTGAGCGGGCAGAGATGATGGAGCTCAATGACCGCTTT
GCCAGCTACATCGAGAAGGTTCGCTTCCTGGAACAGCAAAACAAGGCGCTGGCTGCTGAG
CTGAACCAGCTGCGGGCCAAGGAGCCCACCAAGCTGGCAGACGTCTACCAGGCTGAGCTG
CGAGAGCTGCGGCTGCGGCTCGATCAACTCACCGCCAACAGCGCCCGGCTGGAGGTTGAG
AGGGACAATCTGGCACAGGACCTGGCCACTGTGAGGCAGAAGCTCCAGGATGAAACCAAC
CTGAGGCTGGAAGCCGAGAACAACCTGGCTGCCTATAGACAGGAAGCAGATGAAGCCACC
CTGGCCCGTCTGGATCTGGAGAGGAAGATTGAGTCGCTGGAGGAGGAGATCCGGTTCTTG
AGGAAGATCCACGAGGAGGAGGTTCGGGAACTCCAGGAGCAGCTGGCCCGACAGCAGGTC
CATGTGGAGCTTGACGTGGCCAAGCCAGACCTCACCGCAGCCCTGAAAGAGATCCGCACG
CAGTATGAGGCAATGGCGTCCAGCAACATGCATGAAGCCGAAGAGTGGTACCGCTCCAAG
TTTGCAGACCTGACAGACGCTGCTGCCCGCAACGCGGAGCTGCTCCGCCAGGCCAAGCAC
GAAGCCAACGACTACCGGCGCCAGTTGCAGTCCTTGACCTGCGACCTGGAGTCTCTGCGC
GGCACGAACGAGTCCCTGGAGAGGCAGATGCGCGAGCAGGAGGAGCGGCACGTGCGGGAG
GCGGCCAGTTATCAGGAGGCGCTGGCGCGGCTGGAGGAAGAGGGGCAGAGCCTCAAGGAC
GAGATGGCCCGCCACTTGCAGGAGTACCAGGACCTGCTCAATGTCAAGCTGGCCCTGGAC
ATCGAGATCGCCACCTACAGGAAGCTGCTAGAGGGCGAGGAGAACCGGATCACCATTCCC
GTGCAGACCTTCTCCAACCTGCAGATTCGAGAAACCAGCCTGGACACCAAGTCTGTGTCA
GAAGGCCACCTCAAGAGGAACATCGTGGTGAAGACCGTGGAGATGCGGGATGGAGAGGTC
ATTAAGGAGTCCAAGCAGGAGCACAAGGATGTGATGTGA

Clone variation with respect to NM_002055.4
141 g=>a
5' Read Nucleotide Sequence
>OriGene 5' read for NM_002055 unedited
GCCCCGTTGCCGCAAAGGGCGGTAGGCGTGTACGGTGGGAGGTCTATATAAGCAGAGCTC
ATTTAGGTGACACTATAGAATACAAGCTACTTGTTCTTTTTGCAGCGGCCGCGAATTCGG
CACGAGGGCAGGATGGAGAGGAGACGCATCACCTCCGCTGCTCGCCGCTCCTACGTCTCC
TCAGGGGAGATGATGGTGGGGGGCCTGGCTCCTGGCCGCCGTCTGGGTCCTGGCACCCGC
CTCTCCCTGGCTCGAATGCCCCCTCCACTCCCAACCCGGGTGGATTTCTCCCTGGCTGGG
GCACTCAATGCTGGCTTCAAGGAGACCCGGGCCAGTGAGCGGGCAGAGATGATGGAGCTC
AATGACCGCTTTGCCAGCTACATCGAGAAGGTTCGCTTCCTGGAACAGCAAAACAAGGCG
CTGGCTGCTGAGCTGAACCAGCTGCGGGCCAAGGAGCCCACCAAGCTGGCAGACGTCTAC
CAGGCTGAGCTGCGAGAGCTGCGGCTGCGGCTCGATCAACTCACCGCCAACAGCGCCCGG
CTGGAGGTTGAGAGGGACAATCTGGCACAGGACCTGGCCACTGTGAGGCAGAAGCTCCAG
GATGAAACCAACCTGAGGCTGGAAGCCGAGAACAACCTGGCTGCCTATAGACAGGAAGCA
GATGAAGCCACCCTGGCCCGTCTGGATCTGGAGAGGAAGATTGAGTCGCTGGAGGAGGAG
ATCCGGTTCTTGAGGAAGATCCACGANGAGGGAGGTCGGNAACTNCAGNAGCAGCTGGCC
CGACAGCNAGTCCATGTGGAGCTTGACGTGGCCAGCCAGACCTCACGCAGCCCTGAAAGA
GATCGCACGCAGTATGAGGGCATGGCGTCCAGCACATGCATGAAGCCCGAGAGTGTACCG
CTCCCAGTTGCAGACCTGACGACGCTGCTGNCCGCACGCGNAGCTGNTCCGCCAGGCCAG
CCACGAGCCACGACTACCGNGCCAGNTGCAGTCCTTGACTGCGACCTGNNATCTCTGCNC
GGNACAN
3' Read Nucleotide Sequence
>OriGene 3' read for NM_002055 unedited
TTGGTCGCTGCCGCAATTTANATCGAGTTTTTTTTTTTTTTTTTTGAGGGCGCAGCATTT
GTCTTTATTTTTCCTCAGCGACTAAAGGCAGCAGCAGTGCCCTGAAGATTAGCAGCAGCA
GCAGCAGCAGGTGGCAGGAAGGAGTGGAGGGAAAGGACACCAAGTCTTGGGGAGAGGGAA
GGACCCTTCTTCGGCCTTAGAGGGGAGAGGAGAACCCTGAAGTGGGCCCTCCCAGTCCCA
TCTCTGGGCACAGATCCCACCAGTCTGCTCACCAGTCTGCTCAGTCAAAGCAGAGTGGGT
GCACTGGGGTGGACGTGTCAGCCCTGAGCACCCGGCCTCCAGGCTGCAGGAATATGAGCC
AGTGTCTTCACTTTGCTCGTGCCTCAGTTTTACAATTGTAAAATAGGGCACTACCTAGAA
TACTGGGTACATTTTGTGTGTGAGTAAGAAGGGACCGCAAGAGGCCCTTGGCTTAGGGAA
AAGCAGCCGGTCACTATGGGGTGGAGAGGGTCAGACGTGTGGCAGTGGCTTACTGGGGTT
AAGAAGCAGCAGTCCCAGGGGCTCAGAGGCTGGGGCGGCCTGGTATGACACAGCAAGGAA
GAGGCCTTTAGAAATGGGACAAAGTCATGCCCTGCCCCCATGGATACATCCCCTTTCTCT
CCTGTTTCAGCATCTTCAAGAGGATGAGTCACTTCCTTAATTCCCACAATCCAGAGGCCA
AGTGCAACTGGTCACCCACAACCCCTACTTGTATGCCTAGCGCCATCCCAATTGCCTCCT
CCTCCATCTCTACCAGCGTCCCCTCCAGTCTGCACGGGGCAGTCCTCCTGGGCTTGACCT
CTCTGTACCCACAGCTGGGGGCCAGGCAGCCCCCCTCTATCCCTCCCAGCACTNATCCCT
CTNCACGTACACCACAGATCCCCCCAGTGCTGAGAAATCAAGCTCCACCTGCCCACAGCG
TGCCCACAGATGGCATC
Restriction Sites NotI-NotI |
ACCN NM_002055
Insert Size 3075 bp
OTI Disclaimer Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).
Components The ORF clone is ion-exchange column purified and shipped in a 2D barcoded Matrix tube containing 10ug of transfection-ready, dried plasmid DNA (reconstitute with 100 ul of water).
Reconstitution Method 1. Centrifuge at 5,000xg for 5min.
2. Carefully open the tube and add 100ul of sterile water to dissolve the DNA.
3. Close the tube and incubate for 10 minutes at room temperature.
4. Briefly vortex the tube and then do a quick spin (less than 5000xg) to concentrate the liquid at the bottom.
5. Store the suspended plasmid at -20°C. The DNA is stable for at least one year from date of shipping when stored at -20°C.
Note Plasmids are not sterile.  For experiments where strict sterility is required, filtration with 0.22um filter is required.
Shipping Ambient
Reference Data
RefSeq NM_002055.2, NP_002046.1
RefSeq Size 3035 bp
RefSeq ORF 1299 bp
Locus ID 2670
UniProt ID P14136
Cytogenetics 17q21.31
Domains filament, filament_head
Protein Families ES Cell Differentiation/IPS
Summary This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. Alternative splicing results in multiple transcript variants encoding distinct isoforms. provided by RefSeq, Oct 2008
Transcript Variant: This variant (1) represents the longest transcript and encodes a predominant isoform (1, also known as alpha).
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Documents
Resources
"NM_002055" in other vectors (6)
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RC204548 GFAP (Myc-DDK-tagged)-Human glial fibrillary acidic protein (GFAP), transcript variant 1 10 ug
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RC204548L2 Lenti ORF clone of Human glial fibrillary acidic protein (GFAP), transcript variant 1, mGFP tagged 10 ug
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RC204548L3 Lenti ORF clone of Human glial fibrillary acidic protein (GFAP), transcript variant 1, Myc-DDK-tagged 10 ug
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RC204548L4 Lenti ORF clone of Human glial fibrillary acidic protein (GFAP), transcript variant 1, mGFP tagged 10 ug
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RG204548 GFAP (tGFP-tagged) - Human glial fibrillary acidic protein (GFAP), transcript variant 1 10 ug
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file-alt Citations

Alexander disease GFAP R239C mutant shows increased susceptibility to lipoxidation and elicits mitochondrial dysfunction and oxidative stress
Viedma-Poyatos, González-Jiménez, Pajares et al
Redox Biology (2022) 55, 102415 DOI: 10.1016/j.redox.2022.102415
Cited by 37
AI Summary: OriGene products contributed to this study by providing the human GFAP expression plasmid (pCMV6-XL6-GFAP, Cat# SC118873), which was used to express wild-type GFAP in astrocytic cells for comparison with disease-associated mutants.
Snippet: cells received an equivalent volume of vehicle. Plasmids, mutagenesis and transfection procedures - Expression vectors for human GFAP (pCMV6-XL6-GFAP, SC118873) and GFP-GFAP (EX-D0090-M29) were from Origene and Genecopoeia, respectively. The ORF of GFAP was subcloned into the EcoRI and SacII sites of the pIRES2 DSred-Express2 vector (Clontech) to generate the bicistronic vector RFP//GFAP, from wh
Adult-Onset Alexander Disease: New Causal Sequence Variant in the GFAP Gene
Goerttler, Zanetti, Regoni et al
Neurol Genet (2022) 8 (3), e681 DOI: 10.1212/NXG.0000000000000681
AI Summary: OriGene’s human GFAP plasmid (SC118873) was used as the template to introduce and study the novel GFAP-L58P mutation in HeLa cells, enabling the authors to demonstrate its pathogenic effect in adult-onset Alexander disease.
Snippet: y to be pathogenic.6 To test whether this new mutation c.173T>C;p.L58P in GFAP affects intermediated filament network formation, we introduced the point mutation in the plasmid encoding human GFAP (OriGene Technologies, SC118873 by mutagenesis (QuikChange XL Site-Directed Mutagenesis Kit, Agilent)). HeLa cells were transfected with either GFAP-WT or GFAP-L58P. Forty-eight hours after transfectio;To test whether this new mutation c.173TC;p.L58P in GFAP affects intermediated filament network formation, we introduced the point mutation in the plasmid encoding human GFAP (OriGene Technologies, SC118873 by mutagenesis (QuikChange XL Site-Directed Mutagenesis Kit, Agilent))
FigureFigureFigure
A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease
Ciammola, Sangalli, Sassone et al
Front Neurol (2019) 10, 1124 DOI: 10.3389/fneur.2019.01124
AI Summary: OriGene’s human GFAP plasmid (SC118873) was used to express both wild-type and mutant GFAP proteins in cell studies, enabling functional analysis of the novel GFAP mutation identified in the patient with adult-onset Alexander disease.
Snippet: Plasmid encoding human GFAP was purchased from OriGene Technologies (SC118873). … HeLa cells were grown in Dulbecco's modified Eagle's medium, 10% fetal bovine serum, 1% Pen-Strep, 5% CO2 at 37°C, and transfected using lipofectamine 2000;48 h after transfection the cells were immunostained with mAb #3670 Cell signaling GFAP (1: 300). …
FigureFigure
Site-specific phosphorylation and caspase cleavage of GFAP are new markers of Alexander Disease severity
Battaglia, Beltran, Delic et al
Elife (2019) 8 DOI: 10.7554/eLife.47789
AI Summary: OriGene’s pCMV6-XL6-GFAP plasmid (Cat# SC118873) was used in this study to express and analyze GFAP, enabling investigation of post-translational modifications and aggregation relevant to Alexander Disease severity.
Snippet: recombinant DNA reagent pCMV6-XL6- GFAP Origene Cat# SC118873 peptide, recombinant protein TrueCut Cas9 Protein v2 ThermoFisher Cat# A36499 commercial assay or kit Precision gRNA Synthesis Kit ThermoFisher Cat# A29377 commercial assay or kit Agilent Quikchange II Agilent Cat# 200524
The cysteine residue of glial fibrillary acidic protein is a critical target for lipoxidation and required for efficient network organization
Viedma-Poyatos, de Pablo, Pekny et al
Free Radic. Biol. Med. (2018) 120, 380-394 DOI: 10.1016/j.freeradbiomed.2018.04.007
AI Summary: OriGene contributed to this study by providing the plasmid coding human GFAP (pCMV6-XL6-GFAP, accession number: NM_002055), which was used to investigate the role of the cysteine residue in GFAP modification and filament organization.
Snippet: have been previously described [30]. A plasmid coding human GFAP (pCMV6-XL6 -GFAP, accession number: NM_002055) was obtained from Origene. GFP-GFAP was from Genecopoeia. The bicistronic expression vector
Clinical and immunological characteristics of the spectrum of GFAP autoimmunity: a case series of 22 patients
Iorio, Damato, Evoli et al
J. Neurol. Neurosurg. Psychiatr. (2017)
AI Summary: OriGene products pCMV6-XL6-GFAPα (SC118873) and pCMV6-Entry-GFAPδ (SC325916) were used to transfect HEK-293 cells for cell-based assays, enabling the detection and confirmation of GFAP autoantibodies in patient samples in this study.
Snippet: … HEK-293 cells were transfected with plasmids encoding GFAP homo sapiens transcript variant 1 (SC118873, pCMV6-XL6-GFAPα) and variant 2 (SC325916, pCMV6-Entry-GFAPδ, OriGene) using Lipofectamine 3000 (Invitrogen). ...;... … HEK-293 cells were transfected with plasmids encoding GFAP homo sapiens transcript variant 1 (SC118873, pCMV6-XL6-GFAPα) and variant 2 (SC325916, pCMV6-Entry-GFAPδ, OriGene) using Lipofectamine 3000 (Invitrogen). ...;... … HEK-293 cells were transfected with plasmids encoding GFAP homo sapiens transcript variant 1 (SC118873, pCMV6-XL6-GFAPα) and variant 2 (SC325916, pCMV6-Entry-GFAPδ, OriGene) using Lipofectamine 3000 (Invitrogen).
Showing 1-6 of 8 papers.
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