FHAD1 Polyklonale Antilichaam, HRP-vervoeging

The FHAD1 gene encodes a 1,420 amino acid protein and maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8% of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome. 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.

FHA domain-containing protein 1; Forkhead-associated FHA phosphopeptide binding domain; Forkhead-associated domain-containing protein 1; KIAA1937; RP3-467K16.1; FHAD1_HUMAN.

114827

Cytoplasm, Nucleus

401-500/1412

FHAD1

HRP

KLH conjugated synthetic peptide derived from human FHAD1

ELISA, IHC-P, IHC-F

Purified by Protein A.

1µg/µl

ELISA (1:500-1000), IHC-P (1:200-400), IHC-F (1:100-500)

Aqueous buffered solution containing 0.01M TBS (pH 7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Unmodified

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

114827

Human, Mouse, Rat, Cow, Sheep, Rabbit