POU4F3 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA578116-Each-of-1 | In Stock | ₹ 48,905.50 |
PIPA578116 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 48,905.50
GST (18%): ₹ 8,802.99
Total Price: ₹ 57,708.49
Antigen
POU4F3
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Pou4f3
Gene Alias
brain POU domain gene 3.1; brain-3.1; Brain-3C; brain-specific homeobox POU domain protein 3C; brain-specific homeobox/POU domain protein 3.1; Brain-specific homeobox/POU domain protein 3C; brn3.1; Brn-3.1; brn3c; brn-3c; ddl; DFNA15; dreidel; MGC138412; POU class 4 homeobox 3; POU domain transcription factor Brn3C; POU domain, class 4, transcription factor 3; pou4f3; zfbrn-3.1
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
18998, 5459
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunohistochemistry (Paraffin), Western Blot
Concentration
1.11 mg/mL
Formulation
PBS with 20% glycerol and 0.025% ProClin 300; pH 7
Gene Accession No.
Q15319, Q63955
Gene Symbols
Pou4f3
Immunogen
Recombinant protein encompassing a sequence within the center region of human POU4F3. The exact sequence is proprietary.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Mouse
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Positive Control: HeLa nuclear extract Predicted Reactivity: Rat (98%), Bovine (98%) Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- POU4F3 encodes a member of the POU-domain family of transcription factors
- POU-domain proteins have been observed to play important roles in control of cell identity in several systems
- This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons
- Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15.