Oligonucleotides
Apexbio Technology LLC S. FIR.LUCIF REP GENE KIT 100T
S. FIR.LUCIF REP GENE KIT 100T APEXBIO TECHNOLOGIES
Eagle Biosciences Inc E coli Residual DNA Fragment Analysis Detection Kit (qPCR)
E coli Residual DNA Fragment Analysis Detection Kit (qPCR)
MOLECULAR DEPOT LLC Protein DNA Crystal - 48/1 mL
Crystallization Screen for Protein DNA Complexes is a crystallization screen consisting of 48 unique crystallization reagents that were proven to be successful in crystallizing protein-DNA complexes These 48 reagents were formulated after analyzing over 7000 published protein-DNA crystallization conditions and formulating unique reagents that included critical components for the growth of protein-DNA crystals such as the presence of polyamines PEG of various molecular weights divalent ions various salts reducing agents and other additives For in vitro research use only
Biotium EZH2 / KMT6(EZH2/2536), 0.2mg/mL
This gene encodes a member of the Polycomb-group (PcG) family. PcG family members form multimeric protein complexes, which are involved in maintaining the transcriptional repressive state of genes over successive cell generations. This protein associates with the embryonic ectoderm development protein, the VAV1 oncoprotein, and the X-linked nuclear protein. This protein may play a role in the hematopoietic and central nervous systems. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. 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 abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye colors.
Eagle Biosciences Inc HEK293 Cell Residual DNA Fragment Analysis Detection Kit (qPCR)
HEK293 Cell Residual DNA Fragment Analysis Detection Kit (qPCR)
Biotium SOX9 / SRY-box 9(SOX9/3141R), CF647 conjugate, 0.1mg/mL
Sox genes comprise a family of genes that are related to the mammalian sex-determining gene SRY. These genes similarly contain sequences that encode for the HMG-box domain, which is responsible for the sequence-specific DNA-binding activity. Sox genes encode putative transcriptional regulators implicated in the decision of cell fates during development and the control of diverse developmental processes. SOX9 plays an important role in the normal skeletal development. It may regulate the expression of other genes involved in chondrogenesis by acting as a transcription factor for these genes. 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 abundance targets, because blue dyes have lower fluorescence and can give higher non-specific background than other dye col
Cayman Chemical CXCR3 ntagonIst 6c 10mg
A CXCR3 antagonist; inhibits calcium mobilization induced by CXCL11 in HEK293 cells expressing the human receptor (IC50 = 0.06 µM); selective for CXCR3 over a panel of 14 human G protein-coupled receptors at 10 µM; inhibits CXCR3-mediated migration of isolated human T cells (IC50 = ~100 nM)
Abcam Procainamide hydrochloride, Sodium channel blocker, 10G
MW 271.79 g/mol, Purity >99%. Sodium channel blocker. Specific DNA methyltransferase 1 inhibitor (Ki = 7.2 μM). Antiarrhythmic in vivo. Limited ability to cross the blood-brain barrier.
The product is subject to the following: Abcam Restricted Use Statement
BIOHIPPO AAV-Mecp2-Cre-WPRE-hGH-polyA
Recombinant adeno associated virus expressing Cre under the Mecp2 promoter with WPRE and hGH polyA elements. The Cre dependent configuration enables expression only after recombination, providing precise targeted 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 (T-Cell Marker) (rSPN/1094), CF488A conjugate, 0.1mg/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 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 ab
Biotium SOX9 / SRY-box 9(rSOX9/2288), CF488A conjugate, 0.1mg/mL
The specificity of this monoclonal antibody to its intended target was validated by HuProt™ Array, containing more than 19, 000, full-length human proteins. Plays an important role in the normal skeletal development. May regulate the expression of other genes involved in chondrogenesis by acting as a transcription factor for these genes. Nucleus (Potential). Campomelic dysplasia (CMD1) : Rare, often lethal, dominantly inherited, congenital osteo-chondrodysplasia, associated with male-to-female autosomal sex reversal in two-thirds of the affected karyotypic males. A disease of the newborn characterized by congenital bowing and angulation of long bones, unusually small scapulae, deformed pelvis and spine and a missing pair of ribs. Craniofacial defects such as cleft palate, micrognathia, flat face and hypertelorism are common. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. CF Dyes offer exceptional brightness and phot