You Searched For: 6-FAM+Alkyne

Catalog Number: (10431-126)

Supplier: Bioss

Description: The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Catalog Number: (10431-118)

Supplier: Bioss

Description: The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Catalog Number: (10320-376)

Supplier: Bioss

Description: IFI27.

Catalog Number: (10431-124)

Supplier: Bioss

Description: The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Catalog Number: (10431-120)

Supplier: Bioss

Description: The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Catalog Number: (10320-378)

Supplier: Bioss

Description: IFI27.

Catalog Number: (10233-634)

Supplier: Bioss

Description: Plays an important role in the regulation of cell survival, cell division, angiogenesis, cell differentiation and cell migration. Functions as potent mitogen in vitro (By similarity).

Catalog Number: (10246-354)

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. The FAM63A gene product has been provisionally designated FAM63A pending further characterization.

Catalog Number: (10320-308)

Supplier: Bioss

Description: IFI27.

Catalog Number: (10431-122)

Supplier: Bioss

Description: The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Catalog Number: (10431-116)

Supplier: Bioss

Description: The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Catalog Number: (10233-656)

Supplier: Bioss

Description: Plays an important role in the regulation of cell survival, cell division, angiogenesis, cell differentiation and cell migration. Functions as potent mitogen in vitro (By similarity).

Catalog Number: (10320-306)

Supplier: Bioss

Description: IFI27.

Catalog Number: (77463-004)

Supplier: AAT BIOQUEST INC

Description: 7 dye qPCR calibration plate contains seven spectral calibration plates with seven separate dye standards (TAMRA, SYBR, FAM, JOE, NED, ROX, and VIC).

Catalog Number: (77462-250)

Supplier: AAT BIOQUEST INC

Description: Psoralen TMP Azide is an excellent building block for developing site-specific nucleic acid probes via the well-known click chemistry, i.e., Copper-Catalyzed Alkyne–Azide Cycloaddition (CuAAC).

Catalog Number: (10479-240)

Supplier: Bioss

Description: FAM50A (Family with sequence similarity 50, member A) is a basic protein containing a nuclear localization signal. Its specifc function is unknown. It may be a DNA-binding protein or transcriptional factor.