ARG57890
anti-AAAS / Adracalin antibody
anti-AAAS / Adracalin antibody for Western blot and Human
Overview
| Product Description | Rabbit Polyclonal antibody recognizes AAAS / Adracalin |
|---|---|
| Tested Reactivity | Hu |
| Tested Application | WB |
| Host | Rabbit |
| Clonality | Polyclonal |
| Isotype | IgG |
| Target Name | AAAS / Adracalin |
| Antigen Species | Human |
| Immunogen | Recombinant fusion protein corresponding to aa. 287-546 of Human AAAS (NP_056480.1). |
| Conjugation | Un-conjugated |
| Alternate Names | ADRACALA; ADRACALIN; Aladin; ALADIN; AAASb; Adracalin; AAA; GL003 |
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. | ||||
| Positive Control | HeLa | ||||
| Observed Size | ~ 60 kDa |
Properties
| Form | Liquid |
|---|---|
| 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 | |
|---|---|
| Gene Symbol | AAAS |
| Gene Full Name | achalasia, adrenocortical insufficiency, alacrimia |
| Background | The protein encoded by this gene is a member of the WD-repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia-addisonianism-alacrima syndrome (AAAS), also called triple-A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010] |
| Function | Plays a role in the normal development of the peripheral and central nervous system. [UniProt] |
| Cellular Localization | Nucleus, nuclear pore complex. [UniProt] |
| Calculated MW | 60 kDa |
