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Rabbit Anti-FAM98A antibody
Rabbit Anti-FAM98A antibody
FAM 98A; Family with sequence similarity 98 member A; Hypothetical protein LOC25940; LOC25940; Protein FAM98A; FA98A_HUMAN.
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  • NO.:SL11012R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,Mouse,(predicted: Rat,Chicken,Pig,Cow,Horse,Sheep,)
    Applications:ELISA IHC-P IHC-F Flow-Cyt ICC IF
    concentration:1mg/ml
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Product Name FAM98A
Chinese Name FAM98A蛋白抗体
Alias FAM 98A; Family with sequence similarity 98 member A; Hypothetical protein LOC25940; LOC25940; Protein FAM98A; FA98A_HUMAN.  
Research Area Cardiovascular  Cell biology  immunology  Neurobiology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human, Mouse,  (predicted: Rat, Chicken, Pig, Cow, Horse, Sheep, )
Applications ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 Flow-Cyt=1μg/Test ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 55kDa
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human FAM98A: 251-350/519 
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 Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene. The FAM98 gene product has been provisionally designated FAM98 pending further characterization.

Similarity:
Belongs to the FAM98 family.

SWISS:
Q8NCA5

Gene ID:
25940

Database links:

Entrez Gene: 25940 Human

Entrez Gene: 72722 Mouse

Entrez Gene: 100173593 Orangutan

Entrez Gene: 313873 Rat

SwissProt: Q8NCA5 Human

SwissProt: Q3TJZ6 Mouse

SwissProt: Q5R679 Orangutan

SwissProt: Q5FWT1 Rat

Unigene: 468140 Human

Unigene: 24641 Mouse

Unigene: 12770 Rat



Product Picture
Paraformaldehyde-fixed, paraffin embedded (Human breast carcinoma); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (FAM98A) Polyclonal Antibody, Unconjugated (SL11012R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Paraformaldehyde-fixed, paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (FAM98A) Polyclonal Antibody, Unconjugated (SL11012R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
Blank control: hela(blue), the cells were fixed with 2% paraformaldehyde (10 min) and then permeabilized with ice-cold 90% methanol for 30 min on ice..
Isotype Control Antibody: Rabbit IgG(orange) ; Secondary Antibody: Goat anti-rabbit IgG-PE(white blue), Dilution: 1:200 in 1 X PBS containing 0.5% BSA ; Primary Antibody Dilution: 1μg in 100 μL1X PBS containing 0.5% BSA(green).

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