01-674-423
Claudin 14 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 01-674-423-Each-of-1 | In Stock | ₹ 28,969.50 |
01-674-423 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 28,969.50
GST (18%): ₹ 5,214.51
Total Price: ₹ 34,184.01
Antigen
Claudin 14
Classification
Polyclonal
Conjugate
Unconjugated
Gene
CLDN14
Gene Alias
AI851731; claudin 14; claudin-14; CLDN14; DFNB29; UNQ777/PRO1571
Host Species
Chicken
Purification Method
IgY fraction
Regulatory Status
RUO
Gene ID (Entrez)
23562
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Western Blot
Concentration
1 mg/mL
Formulation
PBS with 0.02% sodium azide
Gene Accession No.
O95500
Gene Symbols
CLDN14
Immunogen
Purified recombinant CLDN14 corresponding to the chromosome 21 gene (Human).
Quantity
500 μg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgY
Related Products
Description
- PA1-9540 detects CLDN14 in human samples
- PA1-9540 has been successfully used in Western blot procedures
- By Western blot, PA1-9540 detects a 26 kDa protein representing CLDN14
- PA1-9540 immunogen is a purified recombinant CLDN14 corresponding to the chromosome 21 gene (Human)
- Tight junctions represent one mode of cell-to-cell adhesion in epithelial or endothelial cell sheets, forming continuous seals around cells and serving as a physical barrier to prevent solutes and water from passing freely through the paracellular space
- These junctions are comprised of sets of continuous networking strands in the outwardly facing cytoplasmic leaflet, with complementary grooves in the inwardly facing extracytoplasmic leaflet
- The protein encoded by this gene, a member of the claudin family, is an integral membrane protein and a component of tight junction strands
- The encoded protein also binds specifically to the WW domain of Yes-associated protein
- Defects in this gene are the cause of an autosomal recessive form of nonsyndromic sensorineural deafness
- Several transcript variants encoding the same protein have been found for this gene.