Review




Structured Review

Promega powerplex 16hs multiplex str system
Powerplex 16hs Multiplex Str System, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/powerplex 16hs multiplex str system/product/Promega
Average 90 stars, based on 1 article reviews
powerplex 16hs multiplex str system - by Bioz Stars, 2026-06
90/100 stars

Images



Similar Products

90
Promega powerplex 16hs multiplex str system
Powerplex 16hs Multiplex Str System, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/powerplex 16hs multiplex str system/product/Promega
Average 90 stars, based on 1 article reviews
powerplex 16hs multiplex str system - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

90
Source BioScience plc powerplex str 16hs
Powerplex Str 16hs, supplied by Source BioScience plc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/powerplex str 16hs/product/Source BioScience plc
Average 90 stars, based on 1 article reviews
powerplex str 16hs - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

90
Promega powerplex str 16hs
Powerplex Str 16hs, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/powerplex str 16hs/product/Promega
Average 90 stars, based on 1 article reviews
powerplex str 16hs - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

90
Promega autosomal str kit powerplex®16hs
<t>Autosomal</t> <t>STR</t> genotyping cells removed by microdissection: (a) the genotype of the A blood-type sperm cell; (b) the genotype of the B blood-type sperm cell.
Autosomal Str Kit Powerplex®16hs, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/autosomal str kit powerplex®16hs/product/Promega
Average 90 stars, based on 1 article reviews
autosomal str kit powerplex®16hs - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

90
Promega str profiling powerplex 16hs
<t>Autosomal</t> <t>STR</t> genotyping cells removed by microdissection: (a) the genotype of the A blood-type sperm cell; (b) the genotype of the B blood-type sperm cell.
Str Profiling Powerplex 16hs, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/str profiling powerplex 16hs/product/Promega
Average 90 stars, based on 1 article reviews
str profiling powerplex 16hs - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

90
Promega powerplex 16hs multiplex str dna profiling
NLTB-transduced CB cells do not develop into clonally rearranged leukemias in vitro. a , b BIOMED-2 TCRG clonality assay. a CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders for up to 28 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets of cells were FACS sorted and genomic <t>DNA</t> extracted for analysis. No dominant peaks indicative of clonal T-cell populations were identified in any of these samples. b Doubly transduced (G+C+) CB cells were FACS sorted from day 24 in vitro cultures, as well as from the leukemic mice into which the cultured cells were injected. Genomic DNA was then extracted, and the distribution of amplified TCRG DNA fragments analyzed by GeneScan (Applied Biosystems). Dotted red lines are overlaid to facilitate comparison of peak sizes between samples. Peak sizes are reproducible within less than 0.5 bp. c <t>STR</t> profiling of CB leukemias. Genomic DNAs from primary CB leukemias were profiled by Promega <t>PowerPlex</t> <t>16HS</t> assay. STR patterns from four different individual donors (A, B1, C, D) can be discerned. The minor B2 pattern was not represented after serial transplant. d ImmunoSEQ TCRG clonality assay. CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders. Culture samples were taken at 14, 28, and 38 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets were FACS sorted and genomic DNA extracted for ImmunoSEQ TCRG (Survey) analysis by Adaptive Biotechnologies. Stacked reads are plotted for the 25 most frequent rearrangements with each alternating color indicating a unique, clonally rearranged CDR3 DNA fragment
Powerplex 16hs Multiplex Str Dna Profiling, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/powerplex 16hs multiplex str dna profiling/product/Promega
Average 90 stars, based on 1 article reviews
powerplex 16hs multiplex str dna profiling - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

90
Promega str profiling analysis powerplex 16hs system
NLTB-transduced CB cells do not develop into clonally rearranged leukemias in vitro. a , b BIOMED-2 TCRG clonality assay. a CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders for up to 28 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets of cells were FACS sorted and genomic <t>DNA</t> extracted for analysis. No dominant peaks indicative of clonal T-cell populations were identified in any of these samples. b Doubly transduced (G+C+) CB cells were FACS sorted from day 24 in vitro cultures, as well as from the leukemic mice into which the cultured cells were injected. Genomic DNA was then extracted, and the distribution of amplified TCRG DNA fragments analyzed by GeneScan (Applied Biosystems). Dotted red lines are overlaid to facilitate comparison of peak sizes between samples. Peak sizes are reproducible within less than 0.5 bp. c <t>STR</t> profiling of CB leukemias. Genomic DNAs from primary CB leukemias were profiled by Promega <t>PowerPlex</t> <t>16HS</t> assay. STR patterns from four different individual donors (A, B1, C, D) can be discerned. The minor B2 pattern was not represented after serial transplant. d ImmunoSEQ TCRG clonality assay. CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders. Culture samples were taken at 14, 28, and 38 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets were FACS sorted and genomic DNA extracted for ImmunoSEQ TCRG (Survey) analysis by Adaptive Biotechnologies. Stacked reads are plotted for the 25 most frequent rearrangements with each alternating color indicating a unique, clonally rearranged CDR3 DNA fragment
Str Profiling Analysis Powerplex 16hs System, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/str profiling analysis powerplex 16hs system/product/Promega
Average 90 stars, based on 1 article reviews
str profiling analysis powerplex 16hs system - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

99
Thermo Fisher str dna typing kits powerplex 16hs
NLTB-transduced CB cells do not develop into clonally rearranged leukemias in vitro. a , b BIOMED-2 TCRG clonality assay. a CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders for up to 28 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets of cells were FACS sorted and genomic <t>DNA</t> extracted for analysis. No dominant peaks indicative of clonal T-cell populations were identified in any of these samples. b Doubly transduced (G+C+) CB cells were FACS sorted from day 24 in vitro cultures, as well as from the leukemic mice into which the cultured cells were injected. Genomic DNA was then extracted, and the distribution of amplified TCRG DNA fragments analyzed by GeneScan (Applied Biosystems). Dotted red lines are overlaid to facilitate comparison of peak sizes between samples. Peak sizes are reproducible within less than 0.5 bp. c <t>STR</t> profiling of CB leukemias. Genomic DNAs from primary CB leukemias were profiled by Promega <t>PowerPlex</t> <t>16HS</t> assay. STR patterns from four different individual donors (A, B1, C, D) can be discerned. The minor B2 pattern was not represented after serial transplant. d ImmunoSEQ TCRG clonality assay. CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders. Culture samples were taken at 14, 28, and 38 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets were FACS sorted and genomic DNA extracted for ImmunoSEQ TCRG (Survey) analysis by Adaptive Biotechnologies. Stacked reads are plotted for the 25 most frequent rearrangements with each alternating color indicating a unique, clonally rearranged CDR3 DNA fragment
Str Dna Typing Kits Powerplex 16hs, supplied by Thermo Fisher, 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/result/str dna typing kits powerplex 16hs/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
str dna typing kits powerplex 16hs - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier

90
Promega short tandem repeat (str) kit promega’s powerplex 16hs chemistry
NLTB-transduced CB cells do not develop into clonally rearranged leukemias in vitro. a , b BIOMED-2 TCRG clonality assay. a CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders for up to 28 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets of cells were FACS sorted and genomic <t>DNA</t> extracted for analysis. No dominant peaks indicative of clonal T-cell populations were identified in any of these samples. b Doubly transduced (G+C+) CB cells were FACS sorted from day 24 in vitro cultures, as well as from the leukemic mice into which the cultured cells were injected. Genomic DNA was then extracted, and the distribution of amplified TCRG DNA fragments analyzed by GeneScan (Applied Biosystems). Dotted red lines are overlaid to facilitate comparison of peak sizes between samples. Peak sizes are reproducible within less than 0.5 bp. c <t>STR</t> profiling of CB leukemias. Genomic DNAs from primary CB leukemias were profiled by Promega <t>PowerPlex</t> <t>16HS</t> assay. STR patterns from four different individual donors (A, B1, C, D) can be discerned. The minor B2 pattern was not represented after serial transplant. d ImmunoSEQ TCRG clonality assay. CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders. Culture samples were taken at 14, 28, and 38 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets were FACS sorted and genomic DNA extracted for ImmunoSEQ TCRG (Survey) analysis by Adaptive Biotechnologies. Stacked reads are plotted for the 25 most frequent rearrangements with each alternating color indicating a unique, clonally rearranged CDR3 DNA fragment
Short Tandem Repeat (Str) Kit Promega’s Powerplex 16hs Chemistry, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/short tandem repeat (str) kit promega’s powerplex 16hs chemistry/product/Promega
Average 90 stars, based on 1 article reviews
short tandem repeat (str) kit promega’s powerplex 16hs chemistry - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

Image Search Results


Autosomal STR genotyping cells removed by microdissection: (a) the genotype of the A blood-type sperm cell; (b) the genotype of the B blood-type sperm cell.

Journal: BioMed Research International

Article Title: Sperm Cell Capture Based on ABH Antigen Differences to Separate Two Men in Mixed Seminal Stains

doi: 10.1155/2021/7269237

Figure Lengend Snippet: Autosomal STR genotyping cells removed by microdissection: (a) the genotype of the A blood-type sperm cell; (b) the genotype of the B blood-type sperm cell.

Article Snippet: An autosomal STR kit (PowerPlex®16HS, Promega) was used to amplify 15 autosomal STR loci via PCR, according to the manufacturer's recommendations.

Techniques: Laser Capture Microdissection

NLTB-transduced CB cells do not develop into clonally rearranged leukemias in vitro. a , b BIOMED-2 TCRG clonality assay. a CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders for up to 28 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets of cells were FACS sorted and genomic DNA extracted for analysis. No dominant peaks indicative of clonal T-cell populations were identified in any of these samples. b Doubly transduced (G+C+) CB cells were FACS sorted from day 24 in vitro cultures, as well as from the leukemic mice into which the cultured cells were injected. Genomic DNA was then extracted, and the distribution of amplified TCRG DNA fragments analyzed by GeneScan (Applied Biosystems). Dotted red lines are overlaid to facilitate comparison of peak sizes between samples. Peak sizes are reproducible within less than 0.5 bp. c STR profiling of CB leukemias. Genomic DNAs from primary CB leukemias were profiled by Promega PowerPlex 16HS assay. STR patterns from four different individual donors (A, B1, C, D) can be discerned. The minor B2 pattern was not represented after serial transplant. d ImmunoSEQ TCRG clonality assay. CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders. Culture samples were taken at 14, 28, and 38 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets were FACS sorted and genomic DNA extracted for ImmunoSEQ TCRG (Survey) analysis by Adaptive Biotechnologies. Stacked reads are plotted for the 25 most frequent rearrangements with each alternating color indicating a unique, clonally rearranged CDR3 DNA fragment

Journal: Nature Communications

Article Title: Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia

doi: 10.1038/s41467-019-10510-8

Figure Lengend Snippet: NLTB-transduced CB cells do not develop into clonally rearranged leukemias in vitro. a , b BIOMED-2 TCRG clonality assay. a CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders for up to 28 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets of cells were FACS sorted and genomic DNA extracted for analysis. No dominant peaks indicative of clonal T-cell populations were identified in any of these samples. b Doubly transduced (G+C+) CB cells were FACS sorted from day 24 in vitro cultures, as well as from the leukemic mice into which the cultured cells were injected. Genomic DNA was then extracted, and the distribution of amplified TCRG DNA fragments analyzed by GeneScan (Applied Biosystems). Dotted red lines are overlaid to facilitate comparison of peak sizes between samples. Peak sizes are reproducible within less than 0.5 bp. c STR profiling of CB leukemias. Genomic DNAs from primary CB leukemias were profiled by Promega PowerPlex 16HS assay. STR patterns from four different individual donors (A, B1, C, D) can be discerned. The minor B2 pattern was not represented after serial transplant. d ImmunoSEQ TCRG clonality assay. CB cells were transduced with N + LTB lentiviruses and cultured on OP9-DL1 feeders. Culture samples were taken at 14, 28, and 38 days. Doubly transduced (G+C+) and nontransduced (G−C−) subsets were FACS sorted and genomic DNA extracted for ImmunoSEQ TCRG (Survey) analysis by Adaptive Biotechnologies. Stacked reads are plotted for the 25 most frequent rearrangements with each alternating color indicating a unique, clonally rearranged CDR3 DNA fragment

Article Snippet: Cell line authentication by PowerPlex 16HS multiplex STR DNA profiling (Promega) was performed by Genetica DNA Laboratories (Burlington, NC).

Techniques: In Vitro, Transduction, Cell Culture, Injection, Amplification, Comparison

Synthetic CB leukemias exhibit clonal evolution in vivo and are highly similar to PDXs. a Venn diagram of single nucleotide variants (SNVs). FACS-sorted G+C+ cells from bone marrow or spleen of a low-level engrafted primary recipient mouse were injected into secondary recipients. G+C+ cells were FACS sorted from clinically morbid secondary recipients and genomic DNA extracted for whole exome sequencing. b Unsupervised hierarchical clustering of synthetic NLTB CB leukemias and PDX T-ALLs based on RNA-seq data. Following batch correction with ComBat, correlation distances (1 − Spearman coefficient) across 39 samples (17 synthetic CB leukemias + 22 PDX) were calculated using the top 1000 variable genes within the PDX sample set. Individual CB donors were discriminated by STR profiling. Darker blue indicates greater similarity. PDX RNA-seq data are from the PRoXe repository (NCBI SRA Accession SRP103099). Color scale indicates (1 − Spearman) correlation distance. Darker blue indicates greater similarity. c TCR clonality by MiXCR analysis of RNA-seq data. Distinct CDR3 regions are indicated by alternating colors within each sample; matching colors across samples are coincidental and do not indicate sequence identity. Mature T-cell control shows polyclonal TRA/TRB. The depicted G+C+ CB leukemias show mono/oligoclonal patterns for TRG/TRD and TRB, respectively. The depicted G+C− CB leukemia shows oligoclonal TRB

Journal: Nature Communications

Article Title: Synthetic modeling reveals HOXB genes are critical for the initiation and maintenance of human leukemia

doi: 10.1038/s41467-019-10510-8

Figure Lengend Snippet: Synthetic CB leukemias exhibit clonal evolution in vivo and are highly similar to PDXs. a Venn diagram of single nucleotide variants (SNVs). FACS-sorted G+C+ cells from bone marrow or spleen of a low-level engrafted primary recipient mouse were injected into secondary recipients. G+C+ cells were FACS sorted from clinically morbid secondary recipients and genomic DNA extracted for whole exome sequencing. b Unsupervised hierarchical clustering of synthetic NLTB CB leukemias and PDX T-ALLs based on RNA-seq data. Following batch correction with ComBat, correlation distances (1 − Spearman coefficient) across 39 samples (17 synthetic CB leukemias + 22 PDX) were calculated using the top 1000 variable genes within the PDX sample set. Individual CB donors were discriminated by STR profiling. Darker blue indicates greater similarity. PDX RNA-seq data are from the PRoXe repository (NCBI SRA Accession SRP103099). Color scale indicates (1 − Spearman) correlation distance. Darker blue indicates greater similarity. c TCR clonality by MiXCR analysis of RNA-seq data. Distinct CDR3 regions are indicated by alternating colors within each sample; matching colors across samples are coincidental and do not indicate sequence identity. Mature T-cell control shows polyclonal TRA/TRB. The depicted G+C+ CB leukemias show mono/oligoclonal patterns for TRG/TRD and TRB, respectively. The depicted G+C− CB leukemia shows oligoclonal TRB

Article Snippet: Cell line authentication by PowerPlex 16HS multiplex STR DNA profiling (Promega) was performed by Genetica DNA Laboratories (Burlington, NC).

Techniques: In Vivo, Injection, Sequencing, RNA Sequencing, Control