STAR Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)
-
- Antigène Voir toutes STAR Protéines
- STAR (Steroidogenic Acute Regulatory Protein (STAR))
- Type de proteíne
- Recombinant
- Attributs du protein
- Transcript Variant 2
-
Origine
- Humain
-
Source
- HEK-293 Cells
- Purification/Conjugué
- Cette STAR protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
-
- Recombinant human Steroidogenic acute regulatory protein (STAR), nuclear gene encoding mitochondrial protein, transcript variant 2 (transcript variant 2) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product STAR Protéine
-
-
- Indications d'application
-
Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
-
The tag is located at the C-terminal.
- Restrictions
- For Research Use only
-
- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
-
- Antigène
- STAR (Steroidogenic Acute Regulatory Protein (STAR))
- Abstract
- STAR Produits
- Synonymes
- STARD1 Protein, AV363654 Protein, D8Ertd419e Protein, star Protein, LOC100219165 Protein, StARD1 Protein, steroidogenic acute regulatory protein Protein, steroidogenic acute regulatory protein L homeolog Protein, STAR Protein, Star Protein, star Protein, star.L Protein
- Sujet
- 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.
- Poids moléculaire
- 29.9 kDa
- NCBI Accession
- NP_001007244
- Pathways
- Metabolism of Steroid Hormones and Vitamin D, Response to Growth Hormone Stimulus, C21-Steroid Hormone Metabolic Process, Cellular Response to Molecule of Bacterial Origin, Carbohydrate Homeostasis
-