Connexin 26 Recombinant Mouse Monoclonal Antibody (24F5), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA550243-Each-of-1 | In Stock | ₹ 37,202.00 |
FEMA550243 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 37,202.00
GST (18%): ₹ 6,696.36
Total Price: ₹ 43,898.36
Antigen
Connexin 26
Classification
Recombinant Monoclonal
Concentration
1 mg/mL
Formulation
PBS with 50% glycerol and 0.03% Proclin 300, pH 7.4
Gene Accession No.
P29033
Gene Symbols
Gjb2
Immunogen
Recombinant Human GJB2 protein
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
Applications
ELISA, Flow Cytometry, Immunohistochemistry (Paraffin)
Clone
24F5
Conjugate
Unconjugated
Gene
Gjb2
Gene Alias
AI325222, Cnx26, connexin 26, connexin-26, CX26, CXN-26, DFNA3, DFNA3A, DFNB1, DFNB1A, Gap junction beta-2 protein, gap junction channel protein connexin 26, gap junction membrane channel protein beta 2, gap junction protein beta 2, gap junction protein, beta 2, gap junction protein, beta 2, 26kDa, GJB2, Gjb-2, HID, KID, mutant gap junction protein beta 2, NSRD1, PPK
Host Species
Mouse
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
2706
Content And Storage
-20°C or -80°C if preferred
Isotype
IgG
Related Products
Description
- Gap junctions are conduits that allow the direct cell-to-cell passage of small cytoplasmic molecules, including ions, metabolic intermediates, and second messengers, and thereby mediate intercellular metabolic and electrical communication
- Gap junction channels consist of connexin protein subunits, which are encoded by a multigene family
- GJBs (gap-junction proteins or connexins) play crucial functional roles associated with these channels
- Defects in GJB3 have been linked to erythrokeratodermia variables (EKV) is an autosomal dominant genodermatosis characterized by transient figurate red patches or hyperkeratosis
- Mutations in GJB2 have also been associated with genetically derived hearing impairments, including autosomal recessive nonsyndromic deafness.