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chromatography+columns+HyClone+products+(Cytiva)
Supplier:
AGILENT TECHNOLOGIES, INC (CSD) CA
Description:
Fittings and connectors for Agilent 7700, 7800, 7900, 8800, 8900 ICP-MS including ISIS switching valve.
Supplier:
Spectrum Chemicals
Description:
Manganese Sulfate, Monohydrate, Powder, FCC, BP - The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.
Supplier:
AGILENT TECHNOLOGIES, INC (CSD) CA
Description:
Plug and play Easy-fit torches for the 4100, 4200 and 4210 MP-AES Instruments.
Catalog Number:
(10493-400)
Supplier:
Bioss
Description:
C14orf106 is required for recruitment of CENPA to centromeres and normal chromosome segregation during mitosis. It interacts with SP1. There are two isoforms.Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5% of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14;19) translocations found in a variety of B cell malignancies. The C14orf106 gene product has been provisionally designated C14orf106 pending further characterization.
Catalog Number:
(10492-596)
Supplier:
Bioss
Description:
Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf70 gene product has been provisionally designated C8orf70 pending further characterization.
Catalog Number:
(10108-096)
Supplier:
Prosci
Description:
The function remains unknown.
Catalog Number:
(10101-848)
Supplier:
Prosci
Description:
The function of SCML1 remains unknown.
Catalog Number:
(10108-424)
Supplier:
Prosci
Description:
The function remains unknown.
Catalog Number:
(89311-186)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to CBLC (Cas-Br-M (murine) ecotropic retroviral transforming sequence c)
Catalog Number:
(CA600-446-384)
Supplier:
Rockland Immunochemical
Description:
Primary Rabbit Anti-HA EPITOPE TAG Reacts with Pan
Catalog Number:
(CA600-446-382)
Supplier:
Rockland Immunochemical
Description:
Primary Rabbit Anti-6X HIS EPITOPE TAG Reacts with Pan
Catalog Number:
(CA600-441-381)
Supplier:
Rockland Immunochemical
Description:
Primary Rabbit Anti-MYC EPITOPE TAG Reacts with Pan
Catalog Number:
(CA600-442-383)
Supplier:
Rockland Immunochemical
Description:
Primary Rabbit Anti-FLAG™ conjugated proteins Reacts with Pan
Catalog Number:
(CA600-442-382)
Supplier:
Rockland Immunochemical
Description:
Primary Rabbit Anti-6X HIS EPITOPE TAG Reacts with Pan
Catalog Number:
(10457-978)
Supplier:
Bioss
Description:
CCDC17, also known as FLJ17921 or RP4-697E16.4, is a 622 amino acid protein expressed as four 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:
(CA76470-764)
Supplier:
New England Biolabs (NEB)
Description:
Plastic parts for retaining the Monarch DNA capture beads during the Monarch HMW DNA extraction workflow. These pieces resemble spin columns without any membrane inserted and facilitate various steps of the extraction workflow. They mate to the Monarch collection tube II.
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