Oligonucleotides
BIOHIPPO AAV-hSyn-Cre-P2A-hChR2(H134R)-EYFP-WPREs
Recombinant adeno associated virus expressing Cre hChR2(H134R) fused to EYFP under the hSyn promoter with WPRE and hGH polyA elements. The Cre dependent configuration enables expression only after recombination, providing precise optogenetic control of targeted neurons. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
Biotium CD43(SPN/1094), 0.2mg/mL
This antibody recognizes a cell surface glycoprotein of 95/115/135 kDa (depending upon the extent of glycosylation), identified as CD43. 70-90% of T-cell lymphomas and from 22-37% of B-cell lymphomas express CD43. No reactivity has been observed with reactive B-cells. So a B-lineage population that co-expresses CD43 is highly likely to be a malignant lymphoma, especially a low-grade lymphoma, rather than a reactive B-cell population. When CD43 antibody is used in combination with anti-CD20, effective immunophenotyping of the lymphomas in formalin-fixed tissues can be obtained. Co-staining of a lymphoid infiltrate with anti-CD20 and anti-CD43 argues against a reactive process and favors a diagnosis of lymphoma.Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and photostability. Note: Conjugates of blue fluorescent dyes like CF405S and CF405M are not recommended for detecting low abundan
ABclonal Technology AFTMag Quick Plant Leaf DNA Extraction Kit (Prepackaged)
This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction.
ABclonal Technology RK21623-5uleach Unique Dual I
ABclonal s Unique Dual Index for Illumina products contain universal truncated adapters and Unique Dual Index (UDI) primers for sample preparation for Next Generation Sequencing on Illumina sequencing The MidiSet (CAT NO RK21623) provides 24 unique primer pairs (UDI Primers 1-24) All sets include 15 M truncated adapters along with the listed primers The sample index length is 8 nucleotides
