PIPA595685
Phospho-FANCI (Ser559) Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA595685-Each-of-1 | In Stock | ₹ 48,905.50 |
PIPA595685 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 48,905.50
GST (18%): ₹ 8,802.99
Total Price: ₹ 57,708.49
Antigen
Phospho-FANCI (Ser559)
Classification
Polyclonal
Conjugate
Unconjugated
Gene
FANCI
Gene Alias
FANCI, Fanconi anemia complementation group I, Fanconi anemia group I protein, Fanconi anemia group I protein homolog, Fanconi anemia, complementation group I, KIAA1794, Protein FACI
Host Species
Rabbit
Purification Method
Antigen Affinity Chromatography
Regulatory Status
RUO
Gene ID (Entrez)
55215
Content And Storage
-20°, C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
Western Blot
Concentration
∽0.15 mg/mL
Formulation
10mM HEPES with 100μg/mL BSA, 150mM NaCl, 50% glycerol and no preservative, pH 7.5
Gene Accession No.
Q9NVI1
Gene Symbols
FANCI
Immunogen
Synthetic phospho-peptide corresponding to amino acid residues surrounding Ser556 conjugated to KLH
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Antigen Affinity Purified from Pooled Serum The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2)
- The previously defined group FANCH is the same as FANCA
- Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair
- The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex
- This gene encodes the protein for complementation group I
- Alternative splicing results in two transcript variants encoding different isoforms.