Review



dh5α  (New England Biolabs)


Bioz Verified Symbol New England Biolabs is a verified supplier
Bioz Manufacturer Symbol New England Biolabs manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 99

    Structured Review

    New England Biolabs dh5α
    Dh5α, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 3016 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5-alpha+Competent+E%2E+coli/pmc12796543-239-6-7
    Average 99 stars, based on 3016 article reviews
    dh5α - by Bioz Stars, 2026-09
    99/100 stars

    Images

    Related Articles

    Polymerase Chain Reaction:

    Article Title: Profiling of DNA-methylation signatures in human ILCs during homeostasis and allergic disease
    Article Snippet: Differentially methylated regions (DMRs) and the corresponding promoter region from the HPGDS locus and CRTH2 promoter region containing the enhancer element, as described by , were cloned into the pNL1.1-NanoLuc vector (Promega). .. To this end, PCR-amplified fragments from human PBMC-derived genomic DNA were digested alongside the luciferase vector with compatible restriction enzymes, gel-purified, ligated using T4 DNA ligase (NEB), and transformed into NEB 5-alpha E. coli . ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose.
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Luciferase:

    Article Title: Profiling of DNA-methylation signatures in human ILCs during homeostasis and allergic disease
    Article Snippet: Differentially methylated regions (DMRs) and the corresponding promoter region from the HPGDS locus and CRTH2 promoter region containing the enhancer element, as described by , were cloned into the pNL1.1-NanoLuc vector (Promega). .. To this end, PCR-amplified fragments from human PBMC-derived genomic DNA were digested alongside the luciferase vector with compatible restriction enzymes, gel-purified, ligated using T4 DNA ligase (NEB), and transformed into NEB 5-alpha E. coli . ..

    Plasmid Preparation:

    Article Title: Profiling of DNA-methylation signatures in human ILCs during homeostasis and allergic disease
    Article Snippet: Differentially methylated regions (DMRs) and the corresponding promoter region from the HPGDS locus and CRTH2 promoter region containing the enhancer element, as described by , were cloned into the pNL1.1-NanoLuc vector (Promega). .. To this end, PCR-amplified fragments from human PBMC-derived genomic DNA were digested alongside the luciferase vector with compatible restriction enzymes, gel-purified, ligated using T4 DNA ligase (NEB), and transformed into NEB 5-alpha E. coli . ..

    Article Title: Prototyping Minimal Extracellular Vesicle Mimetics Using Cell-Free Synthesis.
    Article Snippet: The generated plasmids were transformed into NEB 5-alpha Competent E. coli (C2987H, New England Biolabs). .. Transformation was performed by incubating 10 ng of the plasmid with 10 μL of competent NEB 5-alpha E. coli for 30 min on ice. .. The cells underwent a 42 °C heat shock for 30 s, placed back on ice for 5 min then resuspended in 2x YT media and incubated at 37 °C for 1 h. The cells were centrifuged at 3000g for 5 min to pellet them for concentration, then these cells were plated on 2x YT agar plates (31 g L−1 2x YT, 16 g L−1 agar) (A1672, Millipore Spectrum) and grown at 37 °C overnight.

    Article Title: Modified meiosis in the tardigrade Hypsibius exemplaris maintains heterozygosity across the genome
    Article Snippet: Final products from 2-step PCR performed on pooled tardigrade samples (15-20 animals each) were purified using the Zymoclean Gel DNA Recovery Kit (Zymo D4008) and quantified using Nanodrop. .. Each amplicon was cloned into a pDEST17 Gateway destination vector (Invitrogen 11803012) using the NEBuilder HiFi DNA Assembly Master Mix kit (NEB E2621), and plasmids were transformed into chemically-competent NEB 5-alpha E. coli (NEB C2987), both according to the manufacturer’s protocols. ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose.
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Transformation Assay:

    Article Title: Profiling of DNA-methylation signatures in human ILCs during homeostasis and allergic disease
    Article Snippet: Differentially methylated regions (DMRs) and the corresponding promoter region from the HPGDS locus and CRTH2 promoter region containing the enhancer element, as described by , were cloned into the pNL1.1-NanoLuc vector (Promega). .. To this end, PCR-amplified fragments from human PBMC-derived genomic DNA were digested alongside the luciferase vector with compatible restriction enzymes, gel-purified, ligated using T4 DNA ligase (NEB), and transformed into NEB 5-alpha E. coli . ..

    Article Title: Prototyping Minimal Extracellular Vesicle Mimetics Using Cell-Free Synthesis.
    Article Snippet: The generated plasmids were transformed into NEB 5-alpha Competent E. coli (C2987H, New England Biolabs). .. Transformation was performed by incubating 10 ng of the plasmid with 10 μL of competent NEB 5-alpha E. coli for 30 min on ice. .. The cells underwent a 42 °C heat shock for 30 s, placed back on ice for 5 min then resuspended in 2x YT media and incubated at 37 °C for 1 h. The cells were centrifuged at 3000g for 5 min to pellet them for concentration, then these cells were plated on 2x YT agar plates (31 g L−1 2x YT, 16 g L−1 agar) (A1672, Millipore Spectrum) and grown at 37 °C overnight.

    Article Title: Modified meiosis in the tardigrade Hypsibius exemplaris maintains heterozygosity across the genome
    Article Snippet: Final products from 2-step PCR performed on pooled tardigrade samples (15-20 animals each) were purified using the Zymoclean Gel DNA Recovery Kit (Zymo D4008) and quantified using Nanodrop. .. Each amplicon was cloned into a pDEST17 Gateway destination vector (Invitrogen 11803012) using the NEBuilder HiFi DNA Assembly Master Mix kit (NEB E2621), and plasmids were transformed into chemically-competent NEB 5-alpha E. coli (NEB C2987), both according to the manufacturer’s protocols. ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose.
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Article Title: Investigating and correcting a rare pathogenic mutation in GDF11.
    Article Snippet: Transformations were performed using NEB 5-alpha Competent E. coli (NEB #C2987I) according to manufacturer’s instructions. ngRNA Plasmid Digest – BPK1520 was digested with BsmBI-v2 (NEB #R0739S) at 55°C for 1 h, run on a 1% agarose gel, and the ~2.2 kb fragment was purified (Promega Wizard SV Gel and PCR Clean-Up System, #A9282). pegRNA Plasmid Digest – pU6-pegRNA-GG-acceptor, pU6-tevopreq1-GG-acceptor, and pU6-tmpknot-GG-acceptor were digested with BsaI-HFv2 (NEB #R3733S) at 37°C for 1 h, run on a 1% agarose gel, and the ~2.2 kb fragment was purified. .. Oligo Duplex Annealing – ssDNA oligos for pegRNAs and ngRNAs (IDT; sequences in Supplemental Information) were annealed as described in [5]. ngRNA Cloning – Annealed duplex oligos were ligated into BsmBI-v2-digested BPK1520 using T4 DNA ligase (NEB #M0202), transformed into NEB 5-alpha E. coli, plated on LB-Ampicillin plates, and miniprepped after overnight culture. pegRNA Cloning – Spacer, scaffold, and extension segments were assembled by Golden Gate cloning into BsaI-digested pegRNA plasmids as in [5]. ..

    Amplification:

    Article Title: Modified meiosis in the tardigrade Hypsibius exemplaris maintains heterozygosity across the genome
    Article Snippet: Final products from 2-step PCR performed on pooled tardigrade samples (15-20 animals each) were purified using the Zymoclean Gel DNA Recovery Kit (Zymo D4008) and quantified using Nanodrop. .. Each amplicon was cloned into a pDEST17 Gateway destination vector (Invitrogen 11803012) using the NEBuilder HiFi DNA Assembly Master Mix kit (NEB E2621), and plasmids were transformed into chemically-competent NEB 5-alpha E. coli (NEB C2987), both according to the manufacturer’s protocols. ..

    Clone Assay:

    Article Title: Modified meiosis in the tardigrade Hypsibius exemplaris maintains heterozygosity across the genome
    Article Snippet: Final products from 2-step PCR performed on pooled tardigrade samples (15-20 animals each) were purified using the Zymoclean Gel DNA Recovery Kit (Zymo D4008) and quantified using Nanodrop. .. Each amplicon was cloned into a pDEST17 Gateway destination vector (Invitrogen 11803012) using the NEBuilder HiFi DNA Assembly Master Mix kit (NEB E2621), and plasmids were transformed into chemically-competent NEB 5-alpha E. coli (NEB C2987), both according to the manufacturer’s protocols. ..

    other:

    Article Title: Integrase-On-Demand: bioprospecting integrases for targeted genomic insertion of genetic cargo.
    Article Snippet: Donor (Ec100D pir + cloning trains) and helper (HB101 with conjugal plasmid pRL443) sc heric hia coli strains for cyanobacterial conjugation were ultured at 30 ◦C in LB Lennox medium (Sigma, L3022× 1KG).

    Cell Culture:

    Article Title: Integrase-On-Demand : bioprospecting integrases for targeted genomic insertion of genetic cargo
    Article Snippet: Donor (Ec100D pir + cloning strains) and helper (HB101 with conjugal plasmid pRL443) Escherichia coli strains for cyanobacterial conjugation were cultured at 30°C in LB Lennox medium (Sigma, L3022-6 × 1KG). .. NEB 5-alpha E. coli (NEB, Ipswich, MA, C2987H), NEB 5-alpha F’I q E. coli (NEB, Ipswich, MA, C2992I), and P. putida were cultured in LB medium (Sigma–Aldrich, Darmstadt, Germany, L3522) at 37°C ( E. coli ) or 30°C ( P. putida ). .. When applicable, media were supplemented with 100 μg/ml diaminopimelic acid (DAP; Fisher AAB2239106) ( E. coli ), 50 μg/ml carbenicillin (Sigma C1389-5G; E. coli ), 34 μg/ml of chloramphenicol (Teknova, Hollister, CA, C0322) ( E. coli ), 50 μg/ml kanamycin sulfate (American Bio, AB01100-00010; S. elongatus ), or tetracycline (Teknova, Hollister, CA, T3325) at 10 μg/ml ( E. coli ) or 25 μg/ml ( P. putida ).

    Isolation:

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose.
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Purification:

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Article Title: SPNS2 exports sphingosine-1-phosphate and imports glucose.
    Article Snippet: Briefly, to prepare plasmid DNA templates the coding region of SPNS2 from Human Tagged ORF Clone in pCMV6-AC-GFP (#RG225940, Origene) was inserted into the expression vector pEU-E01-MCS. .. Plasmid DNA template was isolated from transformed NEB 5-alpha E. coli (# C2987H, New England Biolabs) in LB broth with 100 μg/mL ampicillin (#L8105, Teknova) with the Monarch Plasmid Miniprep Kit (#T1010S, New England Biolabs) and further purified with Monarch PCR & DNA Cleanup Kit (#T1030S, New England Biolabs). ..

    Cloning:

    Article Title: Investigating and correcting a rare pathogenic mutation in GDF11.
    Article Snippet: Transformations were performed using NEB 5-alpha Competent E. coli (NEB #C2987I) according to manufacturer’s instructions. ngRNA Plasmid Digest – BPK1520 was digested with BsmBI-v2 (NEB #R0739S) at 55°C for 1 h, run on a 1% agarose gel, and the ~2.2 kb fragment was purified (Promega Wizard SV Gel and PCR Clean-Up System, #A9282). pegRNA Plasmid Digest – pU6-pegRNA-GG-acceptor, pU6-tevopreq1-GG-acceptor, and pU6-tmpknot-GG-acceptor were digested with BsaI-HFv2 (NEB #R3733S) at 37°C for 1 h, run on a 1% agarose gel, and the ~2.2 kb fragment was purified. .. Oligo Duplex Annealing – ssDNA oligos for pegRNAs and ngRNAs (IDT; sequences in Supplemental Information) were annealed as described in [5]. ngRNA Cloning – Annealed duplex oligos were ligated into BsmBI-v2-digested BPK1520 using T4 DNA ligase (NEB #M0202), transformed into NEB 5-alpha E. coli, plated on LB-Ampicillin plates, and miniprepped after overnight culture. pegRNA Cloning – Spacer, scaffold, and extension segments were assembled by Golden Gate cloning into BsaI-digested pegRNA plasmids as in [5]. ..



    Similar Products

    99
    New England Biolabs dh5α
    Dh5α, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5-alpha+Competent+E%2E+coli/pmc12796543-239-6-7
    Average 99 stars, based on 1 article reviews
    dh5α - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    New England Biolabs 5 alpha competent e coli
    UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) <t>Alpha-fold</t> models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.
    5 Alpha Competent E Coli, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5alpha+Comp+E%2Ecoli/pmc13097003-70-1-0
    Average 99 stars, based on 1 article reviews
    5 alpha competent e coli - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    New England Biolabs e coli neb 5 alpha competent cells
    UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) <t>Alpha-fold</t> models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.
    E Coli Neb 5 Alpha Competent Cells, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5alpha+Comp+E%2Ecoli/bio_rxiv__64898__2026__05__08__723909-216-4-6
    Average 99 stars, based on 1 article reviews
    e coli neb 5 alpha competent cells - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    New England Biolabs escherichia coli strain neb 5 alpha
    UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) <t>Alpha-fold</t> models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.
    Escherichia Coli Strain Neb 5 Alpha, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5alpha+Comp+E%2Ecoli/bio_rxiv__64898__2026__05__08__723735-42-0-3
    Average 99 stars, based on 1 article reviews
    escherichia coli strain neb 5 alpha - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    96
    New England Biolabs c2992i e gel96
    UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) <t>Alpha-fold</t> models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.
    C2992i E Gel96, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5-alpha+F+Iq+Comp+E%2Ecoli/pm42102820-723-197-195
    Average 96 stars, based on 1 article reviews
    c2992i e gel96 - by Bioz Stars, 2026-09
    96/100 stars
      Buy from Supplier

    99
    New England Biolabs neb 5 alpha competent cells
    UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) <t>Alpha-fold</t> models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.
    Neb 5 Alpha Competent Cells, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5alpha+Comp+E%2Ecoli/bio_rxiv__64898__2026__04__28__721365-46-33-37
    Average 99 stars, based on 1 article reviews
    neb 5 alpha competent cells - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    99
    New England Biolabs neb 5 alpha e coli
    UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) <t>Alpha-fold</t> models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.
    Neb 5 Alpha E Coli, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/neb+5+alpha+e+coli/NEB+5alpha+Comp+E%2Ecoli/pm42009671-441-7-13
    Average 99 stars, based on 1 article reviews
    neb 5 alpha e coli - by Bioz Stars, 2026-09
    99/100 stars
      Buy from Supplier

    Image Search Results


    UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) Alpha-fold models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.

    Journal: iScience

    Article Title: ISGylation is disrupted by UBA7 gene variants identified in individuals with neurodevelopmental disorder phenotypes

    doi: 10.1016/j.isci.2026.115454

    Figure Lengend Snippet: UBA7 variants from individuals with neurodevelopmental disorders alter protein structure (A) Pedigrees of the families studied in this article indicate the affected individuals 1, 2, and 3. A legend is provided for the symbols used. (B) Diagram of UBA7 protein domains and their functions. The location of the identified variants in the structure is indicated. IAD: inactive adenylation domain, AAD: active adenylation domain, FCCH: first catalytic cysteine half-domain, SCCH: second catalytic cysteine half-domain, UFD: ubiquitin-fold domain. (C) Alpha-fold models of UBA7 protein resulting from UBA7 wild type, or p.Trp311∗ and p.Lys709Serfs∗45 variants. The Red helix represents the added residues resulting from the p.Lys709Serfs∗45 frameshift variant. (D) Structure of wild-type UBA7 in complex with UBE2L6 and ISG15 (left; EMB-16891; pdb: 8OIF ). The top-view (middle) and zoomed areas (right) highlight the adenylation pocket and location of the p.Val548Leu mutation shown in red.

    Article Snippet: NEB 5-alpha Competent E. coli (DH5α) , New England Biolabs , Cat# C2987.

    Techniques: Ubiquitin Proteomics, Variant Assay, Mutagenesis