ARG59075
anti-StAR antibody
anti-StAR antibody for Immunoprecipitation,Western blot and Human,Mouse
Overview
Product Description | Rabbit Polyclonal antibody recognizes StAR |
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Tested Reactivity | Hu, Ms |
Tested Application | IP, WB |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | StAR |
Antigen Species | Human |
Immunogen | Recombinant fusion protein corresponding to aa. 64-285 of Human StAR (NP_000340.2). |
Conjugation | Un-conjugated |
Alternate Names | START domain-containing protein 1; Steroidogenic acute regulatory protein, mitochondrial; STARD1; StAR; StARD1 |
Application Instructions
Predict Reactivity Note | Mouse | ||||||
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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. | ||||||
Observed Size | 35kDa |
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 |
Swiss-port # P49675 Human Steroidogenic acute regulatory protein, mitochondrial Swiss-port # P51557 Mouse Steroidogenic acute regulatory protein, mitochondrial |
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Gene Symbol | STAR |
Gene Full Name | steroidogenic acute regulatory protein |
Background | The protein encoded by this gene plays a key role in the acute regulation of steroid hormone synthesis by enhancing the conversion of cholesterol into pregnenolone. This protein permits the cleavage of cholesterol into pregnenolone by mediating the transport of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane. Mutations in this gene are a cause of congenital lipoid adrenal hyperplasia (CLAH), also called lipoid CAH. A pseudogene of this gene is located on chromosome 13. [provided by RefSeq, Jul 2008] |
Function | Plays a key role in steroid hormone synthesis by enhancing the metabolism of cholesterol into pregnenolone. Mediates the transfer of cholesterol from the outer mitochondrial membrane to the inner mitochondrial membrane where it is cleaved to pregnenolone. [UniProt] |
Cellular Localization | Mitochondrion. [UniProt] |
Calculated MW | 32 kDa |