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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(470164-000)
Supplier:
OSAW INDUSTRIAL PRODUCTS SE
Description:
A useful tool for measuring the magnetic field strength for experiments. The range of the probe is 200 and 2kG with a resolution of 1G at 0 - 200 G. The included probe is a hall probe, which is a flat style probe to fit into small gaps.
Catalog Number:
(CA1.15108.0500)
Catalog Number:
(56620-532)
Supplier:
New Pig
Description:
Contains a user-friendly selection of PIG Socks, Pillows and Mats to absorb up to 24 gallons of liquids
Catalog Number:
(89330-882)
Supplier:
Genetex
Description:
Purity: Purified by antigen-affinity chromatography. Tested Applications: WB-Ag Pkg Size: 100 ul
Catalog Number:
(89306-414)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to LC3A
Catalog Number:
(89363-692)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to Progesterone Receptor
Catalog Number:
(89298-158)
Supplier:
Genetex
Description:
Goat polyclonal antibody to MAD3 / MXD3
Catalog Number:
(89306-512)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to CARM1
Catalog Number:
(89306-468)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to Cyclin B1
Catalog Number:
(89361-606)
Supplier:
Genetex
Description:
Goat polyclonal antibody to SUV39H2
Catalog Number:
(CA82022-846)
Supplier:
G-Biosciences
Description:
Ellman's reagent is a versatile, water-soluble compound for quantifying free sulfhydryl groups in solution. It reacts with a free sulfhydryl group to yield a mixed disulfide and 2-nitro-5-thiobenzoic acid (NTB), a measurable yellow colored product at 412nm.
Ellman's reagent is very useful as a free sulfhydryl assay reagent due to its high specificity for -SH groups at neutral pH, high molar extinction coefficient and short reaction time.
Catalog Number:
(76108-496)
Supplier:
Bioss
Description:
ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia chromosome and the subsequent production of the novel fusion protein BCR-Abl, a potent cell proliferation activator found in several types of leukemias.
Catalog Number:
(76098-890)
Supplier:
Bioss
Description:
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf27 gene product has been provisionally designated C2orf27 pending further characterization.
Catalog Number:
(76100-232)
Supplier:
Bioss
Description:
This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins. The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation. It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair. The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat. Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats. Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and mental retardation. Two transcript variants encoding different isoforms have been found for this gene.
Catalog Number:
(77440-568)
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 CXX1 gene product has been provisionally designated CXX1 pending further characterization.
Catalog Number:
(76098-896)
Supplier:
Bioss
Description:
The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The C2orf39 gene product has been provisionally designated C2orf39 pending further characterization.
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