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chromatography+columns+HyClone+products+(Cytiva)
Catalog Number:
(89354-820)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to CLUAP1 (clusterin-associated protein 1)
Catalog Number:
(89319-848)
Supplier:
Genetex
Description:
Rabbit Polyclonal antibody to GK5 (glycerol kinase 5 (putative))
Supplier:
Veltek Associates
Description:
These headbands are protective and comfortable for using under a bouffant hat in a clean environment.
Catalog Number:
(10100-136)
Supplier:
Prosci
Description:
The exact function of LOC344167 remains unknown.
Catalog Number:
(10100-360)
Supplier:
Prosci
Description:
The exact function of C9orf153 remains unknown.
Catalog Number:
(10108-202)
Supplier:
Prosci
Description:
The exact function of CTA-126B4.3 remains unknown.
Catalog Number:
(10102-680)
Supplier:
Prosci
Description:
The specific function of TRIM67 is not yet known.
Catalog Number:
(10100-236)
Supplier:
Prosci
Description:
The exact functions of C5orf35 remain unknown.
Catalog Number:
(10100-494)
Supplier:
Prosci
Description:
The exact functions of PRR18 remain unknown.
Catalog Number:
(10100-302)
Supplier:
Prosci
Description:
The specific function of CCDC70 is not yet known.
Catalog Number:
(10100-412)
Supplier:
Prosci
Description:
The exact function of C12orf42 remains unknown.
Catalog Number:
(10104-430)
Supplier:
Prosci
Description:
The exact functions of CCDC96 remain unknown.
Catalog Number:
(10493-192)
Supplier:
Bioss
Description:
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:
(10490-870)
Supplier:
Bioss
Description:
Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf192 gene product has been provisionally designated C6orf192 pending further characterization.
Catalog Number:
(10491-014)
Supplier:
Bioss
Description:
Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf174 gene product has been provisionally designated C6orf174 pending further characterization.
Catalog Number:
(10490-942)
Supplier:
Bioss
Description:
Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf120 gene product has been provisionally designated C6orf120 pending further characterization.
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