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Rabbit Anti-FAM63A antibody
Rabbit Anti-FAM63A antibody
FA63A_HUMAN; FAM 63A; FAM63A; Family with sequence similarity 63 member A; FLJ11280; FLJ43504; Hypothetical protein LOC55793; KIAA1390; Protein FAM63A.
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  • NO.:SL11004R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,Mouse,(predicted: Rat,Pig,Cow,Horse,Rabbit,Sheep,)
    Applications:WB ELISA
    concentration:1mg/ml
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Details

Product Name FAM63A
Chinese Name FAM63A蛋白抗体
Alias FA63A_HUMAN; FAM 63A; FAM63A; Family with sequence similarity 63 member A; FLJ11280; FLJ43504; Hypothetical protein LOC55793; KIAA1390; Protein FAM63A.  
Research Area Tumour  Cell biology  immunology  Neurobiology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, Mouse,  (predicted: Rat, Pig, Cow, Horse, Rabbit, Sheep, )
Applications WB=1:500-2000 ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 52kDa
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FAM63A: 151-250/469 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail 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.

Similarity:
Belongs to the FAM63 family.

SWISS:
Q8N5J2

Gene ID:
55793

Database links:

Entrez Gene: 55793 Human

Entrez Gene: 75007 Mouse

Entrez Gene: 310665 Rat

SwissProt: Q8N5J2 Human

SwissProt: Q76LS9 Mouse

SwissProt: Q5BJQ2 Rat

Unigene: 743952 Human

Unigene: 279287 Mouse



Product Picture
Sample:
Liver (Mouse) Lysate at 40 ug
Primary: Anti-FAM63A (SL11004R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 52 kD
Observed band size: 52 kD
Sample:
TT(Human) Cell Lysate at 30 ug
Primary: Anti-FAM63A (SL11004R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 52 kD
Observed band size: 52 kD
Sample:
Embryo (Mouse) Lysate at 40 ug
Primary: Anti-FAM63A (SL11004R) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 52 kD
Observed band size: 52 kD

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