WNT4 Recombinant Rabbit Monoclonal Antibody (HL1889), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA550344-Each-of-1 | In Stock | ₹ 41,385.00 |
FEMA550344 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 41,385.00
GST (18%): ₹ 7,449.30
Total Price: ₹ 48,834.30
Antigen
WNT4
Classification
Recombinant Monoclonal
Concentration
2 mg/mL
Formulation
PBS with no preservative
Gene Accession No.
P56705
Gene Symbols
Wnt4
Immunogen
Recombinant fragment of human Wnt4.
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human, Zebrafish
Form
Liquid
Applications
Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot
Clone
HL1889
Conjugate
Unconjugated
Gene
Wnt4
Gene Alias
protein Wnt-4, SERKAL, signal molecule, UNQ426/PRO864, wingless-related MMTV integration site 4, wingless-type MMTV integration site family member 4, wingless-type MMTV integration site family, member 4, Wnt family member 4, WNT4, Wnt-4
Host Species
Rabbit
Purification Method
Protein A
Regulatory Status
RUO
Gene ID (Entrez)
54361
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Isotype
IgG
Related Products
Description
- The WNT gene family consists of structurally related genes which encode secreted signaling proteins
- These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis
- This gene is a member of the WNT gene family, and is the first signaling molecule shown to influence the sex-determination cascade
- It encodes a protein which shows 98% amino acid identity to the Wnt4 protein of mouse and rat
- This gene and a nuclear receptor known to antagonize the testis-determining factor play a concerted role in both the control of female development and the prevention of testes formation
- This gene and another two family members, WNT2 and WNT7B, may be associated with abnormal proliferation in breast tissue
- Mutations in this gene can result in Rokitansky-Kuster-Hauser syndrome and in SERKAL syndrome.