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Claudin 16 Recombinant monoclonal antibody

Claudin 16 Uni-rAb® Recombinant Antibody for WB, ELISA

Cat No. 82954-2-RR
Clone No.251611H8

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

Claudin-16, CLDN16, Paracellin-1, PCLN1, PCLN-1

Formulation:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
PBS Only
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Tested Applications

Positive WB detected inHEK-293 cells, HepG2 cells, ACHN cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:2000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

82954-2-RR targets Claudin 16 in WB, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen

Peptide

Predict reactive species
Full Name claudin 16
Calculated Molecular Weight 305 aa, 34 kDa
Observed Molecular Weight 34 kDa
GenBank Accession NumberBC069682
Gene Symbol CLDN16
Gene ID (NCBI) 10686
RRIDAB_3743446
Conjugate Unconjugated
FormLiquid
Purification MethodProtein A purification
UNIPROT IDQ9Y5I7
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

Claudins are a family of proteins that are the most important components of the tight junctions, where they establish the paracellular barrier that controls the flow of molecules in the intercellular space between the cells of an epithelium. They have similar structures with four transmembrane domains, with the N-terminus and the C-terminus in the cytoplasm. Claudin-16 is primarily found in the kidneys and is responsible for regulating the reabsorption of magnesium and calcium ions. Mutations in the Claudin-16 gene can lead to a rare genetic disorder called familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC).

Protocols

Product Specific Protocols
WB protocol for Claudin 16 antibody 82954-2-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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