ARG58081
anti-Claudin 11 antibody
anti-Claudin 11 antibody for ICC/IF and Human
Overview
Product Description | Rabbit Polyclonal antibody recognizes Claudin 11 |
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Tested Reactivity | Hu |
Tested Application | ICC/IF |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | Claudin 11 |
Antigen Species | Human |
Immunogen | Recombinant fusion protein corresponding to aa. 26-207 of Human Claudin 11 (NP_005593.2). |
Conjugation | Un-conjugated |
Alternate Names | Oligodendrocyte-specific protein; OSP; OTM; Claudin-11 |
Application Instructions
Application Suggestion |
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Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
Properties
Form | Liquid |
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Purification | Affinity purified. |
Buffer | PBS (pH 7.3), 0.02% Sodium azide and 50% Glycerol. |
Preservative | 0.02% Sodium azide |
Stabilizer | 50% Glycerol |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Gene Symbol | CLDN11 |
Gene Full Name | claudin 11 |
Background | This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Aug 2010] |
Function | Plays a major role in tight junction-specific obliteration of the intercellular space, through calcium-independent cell-adhesion activity. [UniProt] |
Cellular Localization | Cell junction, tight junction, Cell membrane, Multi-pass membrane protein. [UniProt] |
Calculated MW | 22 kDa |