Shopping Cart
Remove All
  • TargetMol
    Your shopping cart is currently empty

Anti-FAM96A Polyclonal Antibody

😃Good
Catalog No. TMAB-05888

Anti-FAM96A Polyclonal Antibody is a Rabbit antibody targeting FAM96A. Anti-FAM96A Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.

Anti-FAM96A Polyclonal Antibody

Anti-FAM96A Polyclonal Antibody

😃Good
Catalog No. TMAB-05888
Anti-FAM96A Polyclonal Antibody is a Rabbit antibody targeting FAM96A. Anti-FAM96A Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 μL$2217-10 days7-10 days
100 μL$3747-10 days7-10 days
200 μL$5277-10 days7-10 days
Add to Cart
Add to Quotation
In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
Questions
TargetMol
View More

Product Introduction

Bioactivity
Description
Anti-FAM96A Polyclonal Antibody is a Rabbit antibody targeting FAM96A. Anti-FAM96A Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.
Ig Type
IgG
Reactivity
Mouse (predicted:Human,Rat,Dog,Cow,Horse,Rabbit,Sheep)
Application
Recommended Dose
IHC-P: 1:100-500; IHC-Fr: 1:100-500; IF: 1:100-500
Antibody Type
Polyclonal
Host SpeciesRabbit
ConstructionPolyclonal Antibody
PurificationProtein A purified
AppearanceLiquid
Formulation0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Concentration1mg/ml
Research BackgroundEncoding 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 FAM96A gene product has been provisionally designated FAM96A pending further characterization.
Antigen Details
Immunogen
KLH conjugated synthetic peptide: human FAM96A
Antigen Species
Human
Gene Name
CIAO2A
Gene ID
Protein Name
Cytosolic iron-sulfur assembly component 2A
Uniprot ID
Chemical Properties
Molecular WeightTheoretical: 18 kDa.
Stability & Storage
Stability & StorageStore at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles.
TransportShipping with blue ice.

Calculator

  • Molarity Calculator
  • Dilution Calculator
  • Reconstitution Calculator
  • Molecular Weight Calculator

Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
Related Tags: buy Anti-FAM96A Polyclonal Antibody | purchase Anti-FAM96A Polyclonal Antibody | Anti-FAM96A Polyclonal Antibody cost | order Anti-FAM96A Polyclonal Antibody | Anti-FAM96A Polyclonal Antibody molecular weight