NFYA Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PA549795-Each-of-1 | In Stock | ₹ 46,502.50 |
PA549795 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 46,502.50
GST (18%): ₹ 8,370.45
Total Price: ₹ 54,872.95
Antigen
NFYA
Classification
Polyclonal
Conjugate
Unconjugated
Gene
NFYA
Gene Alias
AA407810; CAAT box DNA-binding protein subunit A; CAAT-box DNA binding protein subunit A; CAAT-box DNA-binding protein subunit A; CBF-A; Cbf-b; CCAAT-binding transcription factor subunit A; CCAAT-binding transcription factor subunit B; FLJ11236; HAP2; HAP2 CCAAT-binding protein; nf-y; NFYA; NF-YA; Nuclear transcription factor Y subunit A; nuclear transcription factor Y subunit alpha; nuclear transcription factor Y, alpha; nuclear transcription factor-Y alpha; SEZ10; SEZ-10; Transcription factor NF-Y, A subunit
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
18044, 29508, 4800
Content And Storage
-20°C
Form
Liquid
Applications
Western Blot
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4
Gene Accession No.
P18576, P23511, P23708
Gene Symbols
NFYA
Immunogen
Synthesized peptide derived from internal of human NFYA.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse, Rat
Product Type
Antibody
Isotype
IgG
Related Products
Description
- The antibody detects endogenous levels of total NFYA protein
- The SMN1 gene is part of a 500 kb inverted duplication on chromosome 5q13
- This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions
- The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region
- The telomeric and centromeric copies of this gene are nearly identical and encode the same protein - survival motor neuron protein
- The SMN complex plays a catalyst role in the assemble of small nuclear ribonucleoproteins, the building blocks of the spliceosome
- Mutations in the SMN1 gene are known to cause spinal muscular atrophy 1/2.