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Isolation+and+Cleanup+HyClone+products+(Cytiva)
Catalog Number:
(CAPIPA5-18837)
Supplier:
Thermo Scientific
Description:
The product of this gene functions in the nucleotide excision repair pathway, and is required for the repair of DNA lesions such as those induced by UV light or formed by electrophilic compounds including cisplatin. The encoded protein forms a heterodimer with the XPF endonuclease , and the heterodimeric endonuclease catalyzes the 5' incision in the process of excising the DNA lesion. The heterodimeric endonuclease is also involved in recombinational DNA repair and in the repair of inter-strand crosslinks. Mutations in this gene result in cerebrooculofacioskeletal syndrome, and polymorphisms that alter expression of this gene may play a role in carcinogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. The last exon of this gene overlaps with the CD3e molecule, epsilon associated protein gene on the opposite strand.
Catalog Number:
(TCG0118-001G)
Supplier:
TCI America
Description:
Product Categories: Bioscience, Oligopeptides
Other Product Names / Synonyms: H-Gly-Asn-OH
Catalog Number:
(CA72060-064)
Supplier:
Thermo Scientific
Description:
Epredia™ denatured Ethyl Alcohol is formulated to rigid specifications; providing laboratories with a high-quality product. Packaged in high-density polyethylene bottles featuring easy-to-pour design to reduce spills.
Supplier:
TCI America
Description:
Product Categories: Bioscience, Oligopeptides
Other Product Names / Synonyms: L-Carnosine, L-Ignotine
Catalog Number:
(CA89078-694)
Supplier:
Spectrum Chemicals
Description:
Carboxymethylcellulose Sodium, Low Viscosity, Viscosity of 2 Percent Aqueous Solution @ 25 DEG C: 37.5 cP, USP is often used as a thickener and stabilizer. The USP grade indicates it is a grade suitable for personal care, cosmetic and pharmaceutical applications and were manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.
Supplier:
Veltek Associates
Description:
These headbands are protective and comfortable for using under a bouffant hat in a clean environment.
Supplier:
New England Biolabs (NEB)
Description:
Endo Hf is a recombinant protein fusion of Endoglycosidase H and maltose binding protein
Catalog Number:
(CA90000-188)
Supplier:
BD
Description:
Motility Test Medium is a semisolid medium used for the detection of motility of enteric organisms.
Supplier:
Spectrum Chemicals
Description:
Biotin, Powder, USP is a water-soluble B vitamin.
Supplier:
VWR
Description:
Developed exclusively for quantitative face-fit testing to ensure proper worker protection.
Supplier:
Cryopak Verification Technologies
Description:
The iMiniPlus® Dry Ice logger can be programmed to measure extreme temperatures within the range of -100°C to 40°C (-148°F to 104°F)
Supplier:
BD
Description:
BD Difco™ QC Antigens Salmonella O and BD Difco QC Antigen Salmonella Vi are used in the quality control testing of BD Difco Salmonella O Antisera and BD Difco Salmonella Vi Antiserum by slide agglutination tests.
Supplier:
Spectrum Chemicals
Description:
Sodium Citrate, Dihydrate, Granular, USP can be used as an alkalizing agent, buffering agent, emulsifier, or sequestering agent.
Supplier:
Biotium
Description:
This antibody recognizes a protein of 40 kDa, identified as CD7 (also known as gp40, Leu9). CD7 is a member of the immunoglobulin gene superfamily. Its N-terminal amino acids 1-107 are highly homologous to Ig kappa-L chains whereas the carboxyl-terminal region of the extracellular domain is proline-rich and has been postulated to form a stalk from which the Ig domain projects. CD7 is expressed on the majority of immature and mature T-lymphocytes, and T cell leukemia. It is also found on natural killer cells, a small subpopulation of normal B cells and on malignant B cells. Cross-linking surface CD7 positively modulates T cell and NK cell activity as measured by calcium fluxes, expression of adhesion molecules, cytokine secretion and proliferation. CD7 associates directly with phosphoinositol 3'-kinase. CD7 ligation induces production of D-3 phosphoinositides and tyrosine phosphorylation.
CF® dyes are Biotium's next-generation fluorescent dyes. CF®568 is a red fluorescent dye (Ex/Em 562/583 nm) with superior brightness and photostability. It also is compatible with super-resolution imaging by STORM and TIRF.
Catalog Number:
(10478-874)
Supplier:
Bioss
Description:
CCDC18, also known as NY-SAR-41 or dJ717I23.1, is a 1,454 amino acid protein expressed as two isoforms and encoded by a gene mapping to human chromosome 1. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
Catalog Number:
(10478-872)
Supplier:
Bioss
Description:
CCDC18, also known as NY-SAR-41 or dJ717I23.1, is a 1,454 amino acid protein expressed as two isoforms and encoded by a gene mapping to human chromosome 1. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
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