Oligonucleotides
Biotium DNA Ligase 1(1A9), CF647 conjugate, 0.1mg/mL
DNA Ligase I maintains the major DNA Ligase activity in proliferating cells by joining Okazaki fragments during lagging strand DNA replication. Human DNA Ligase I also has an essential role in DNA repair pathways, where it catalyzes the formation of phosphodiester bonds between adjacent 5' phosphoryl and 3' hydroxy termini at single breaks in duplex DNA molecules. In addition, DNA Ligase I plays a role in sealing nicks during excision repair. Similar to other DNA ligases, DNA Ligase I is built around a common catalytic core. Increased levels of DNA Ligase I are found in human tumors, as compared to benign tissues, as well as in peripheral blood lymphocytes. DNA Ligase I activity is altered in the chromosomal breakage deficit Bloom's syndrome (BS). Individuals with BS either have decreased levels of abnormally thermolabile DNA Ligase I or possess a dimeric form of this enzyme. Primary antibodies are available purified, or with a selection of fluorescent CF Dyes and other labels. C
Biotium SOX9 / SRY-box 9(SOX9/2287R), 0.2mg/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
MICRO MEASUREMENT LABORATORIES INC Custom Standard: 100 μm in 1L Bottle
Custom Standard: 100 μm in 1L Bottle
Biomiga Inc. Molecular Biology, Nucleic Acid Extraction, Biomiga, MgPure, Blood Tissue DNA Extraction Kit, genomic DNA, magnetic bead, high-yield purification
Molecular Biology, Nucleic Acid Extraction, Biomiga, MgPure, Blood Tissue DNA Extraction Kit, genomic DNA, magnetic bead, high-yield purification
Biotium SOX9 / SRY-box 9(SOX9/2287R), CF647 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
Medchemexpress LLC Aldolase, Rabbit muscle | 9024-52-6 | 500 U
Aldolase, Rabbit muscle is a glycolytic enzyme and a component of the VATPase complex. It causes fructose 1, 6-diphosphate to decompose into dihydroxyacetone and glyceraldehyde 3-phosphate. This product is for research use only.
- Liquid appearance
- White to off-white color
- EC Number: 4.1.2.13
- Specific activity of ≥10 U/mg protein
- Unit defined by an increase of 1.0 at A240 per minute at 25°C, pH 7.5 with the hydrazine/3-phosphoglyceraldehyde assay
- Classified as an enzyme and biochemical detection enzyme
- Relevant to metabolic and endocrine disease research
- Identified as an endogenous metabolite
Biotium SOX9 / SRY-box 9(rSOX9/2288), CF405S 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
ABclonal Technology POU2F1/OCT1 Rabbit pAb
The OCT1 transcription factor was among the first identified members of the POU transcription factor family (summarized by Sturm et al., 1993 [PubMed 8314572]). Members of this family contain the POU domain, a 160-amino acid region necessary for DNA binding to the octameric sequence ATGCAAAT.
Alkali Scientific DNA & RNA Elution Buffer (EB Buffer) for PCR, Plasmid & Spin Column Cleanup, 500mL
DNA & RNA Elution Buffer is a high-purity solution designed for efficient recovery of nucleic acids during purification workflows. It is commonly used in spin column-based extraction kits for eluting DNA and RNA from silica membranes after washing steps. The buffer is formulated to be PCR compatible, ensuring that eluted nucleic acids can be directly used in downstream applications such as PCR amplification, qPCR, sequencing, and cloning without additional cleanup. Its low ionic strength helps maximize recovery while maintaining nucleic acid stability. This buffer is widely used in molecular biology laboratories for plasmid purification, genomic DNA extraction, and RNA isolation procedures where reliable and contaminant-free elution is required.