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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(89331-128)
Supplier:
Genetex
Description:
Purity: Purified by protein A chromatography or sequential differential precipitations Species Reactivity: Bacteria Tested Applications: ICC/IF Pkg Size: 500 ul
Catalog Number:
(89349-972)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Species Reactivity: Dengue virus Tested Applications: ICC/IF, WB Pkg Size: 100 ul
Catalog Number:
(89331-048)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Species Reactivity: Influenza A virus ( H1N1) Tested Applications: WB Pkg Size: 100 ul
Catalog Number:
(89331-586)
Supplier:
Genetex
Description:
Purity: Purified by protein A chromatography or sequential differential precipitations Species Reactivity: Virus Tested Applications: ELISA Pkg Size: 500 ul
Supplier:
Spectrum Chemicals
Description:
Calcium Hydroxide, Powder, FCC is used extensively in the food industry to clarify solutions, as a digestion aid, baking soda substitute and as a nutritional supplement because of its low toxicity. 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 (FCC) 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:
DWK Life Sciences (KIMBLE)
Description:
These large-opening vials feature a sealed-in, limited-volume insert which allows more consisent sample recovery from vial to vial and reduces the possibility of autosampler needle damage.
Catalog Number:
(89349-888)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to MYH (mutY homolog (E. coli))
Catalog Number:
(89356-052)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to BBS7 (Bardet-Biedl syndrome 7)
Catalog Number:
(89319-834)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to MBNL3 (muscleblind-like 3 (Drosophila))
Catalog Number:
(89321-438)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to Calpain 10 (calpain 10)
Catalog Number:
(89350-022)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to Monoglyceride lipase (monoglyceride lipase)
Catalog Number:
(89318-754)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to RBBP5 (retinoblastoma binding protein 5)
Catalog Number:
(89357-528)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to RCC1 (regulator of chromosome condensation 1)
Catalog Number:
(89349-136)
Supplier:
Genetex
Description:
Rabbit polyclonal antibody to NOTCH2 (Notch homolog 2 (Drosophila))
Catalog Number:
(10479-826)
Supplier:
Bioss
Description:
The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The FAM104B gene product has been provisionally designated FAM104B pending further characterization.
Catalog Number:
(10490-378)
Supplier:
Bioss
Description:
C9orf114 is a 376 amino acid protein encoded by a gene that maps to human chromosome 9q34.11. 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.
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