PEX19 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

N° du produit ABIN2728692

Détail du produit

Antigène: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 1

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette PEX19 protéine est marqué à la Myc-DYKDDDDK Tag.

Application: Antibody Production (AbP), Standard (STD)

Attributs du produit:

• Recombinant human Peroxin 19 / PEX19 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Pureté: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Information d'application

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

Stockage

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.

Détail du antigène

Antigène: PEX19 (Peroxisomal Biogenesis Factor 19 (PEX19))

Autre désignation: Peroxin 19,pex19 (PEX19 Produits)

Synonymes: BEST:GH03076 Protein, CG5325 Protein, DmelPex19 Protein, Dmel\\CG5325 Protein, D1S2223E Protein, HK33 Protein, PBD12A Protein, PMP1 Protein, PMPI Protein, PXF Protein, PXMP1 Protein, Pxf Protein, PxF Protein, Peroxin-19 Protein, Peroxin 19 Protein, Peroxisomal farnesylated protein Protein, peroxisomal biogenesis factor 19 Protein, Pex19 Protein, Bm1_19905 Protein, PEX19 Protein

Sujet: This gene is necessary for early peroxisomal biogenesis. It acts both as a cytosolic chaperone and as an import receptor for peroxisomal membrane proteins (PMPs). Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive, lethal diseases characterized by multiple defects in peroxisome function. These disorders have at least 14 complementation groups, with more than one phenotype being observed for some complementation groups. Although the clinical features of PBD patients vary, cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS), as well as peroxisome biogenesis disorder complementation group 14 (PBD-CG14), which is also known as PBD-CGJ. Alternative splicing results in multiple transcript variants.

Poids moléculaire: 32.6 kDa

NCBI Accession: NP_002848