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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(89330-604)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to Retinoid X Receptor alpha (retinoid X receptor, alpha)
Catalog Number:
(89320-746)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to TXNDC3 (thioredoxin domain containing 3 (spermatozoa))
Catalog Number:
(89354-510)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to KEL (KELl blood group, metallo-endopeptidase)
Catalog Number:
(89320-874)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to PRPS1L1 (phosphoribosyl pyrophosphate synthetase 1-like 1)
Catalog Number:
(89350-404)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to ERK2 (mitogen-activated protein kinase 1)
Catalog Number:
(89321-336)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to ELMO1 (engulfment and cell motility 1)
Catalog Number:
(89294-106)
Supplier:
Genetex
Description:
Goat polyclonal antibody to OMG
Catalog Number:
(CA95022-624)
Supplier:
HiMedia
Description:
Dehydrated culture media for enrichment, isolation, cultivation, and maintenance of microorganisms.
Catalog Number:
(89321-930)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human, Mouse Tested Applications: ICC/IF, IHC-P, WB Pkg Size: 100 ul
Catalog Number:
(10856-082)
Supplier:
Restek
Description:
For use with Agilent 5890 and 6890 GCs.
Catalog Number:
(10854-850)
Supplier:
Restek
Description:
Replacement dessicant cartridge for H2PEM generators.
Catalog Number:
(89323-250)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Species Reactivity: Human Tested Applications: IHC-P, WB Pkg Size: 100 ul
Catalog Number:
(76099-412)
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 C8orf42 gene product has been provisionally designated C8orf42 pending further characterization.
Catalog Number:
(76099-522)
Supplier:
Bioss
Description:
C9orf25 (chromosome 9 open reading frame 25) is a 185 amino acid protein that exists as seven alternatively spliced isoforms that are encoded by a gene located on human chromosome 9. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(10106-286)
Supplier:
Prosci
Description:
The function of the ZNF70 gene has not yet been determined
Catalog Number:
(10100-684)
Supplier:
Prosci
Description:
The function of the C20orf194 gene has not yet been determined.
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