MSH5 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)

N° du produit ABIN2726436

Détail du produit

Antigène: MSH5 (MutS Homolog 5 (MSH5))

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 3

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette MSH5 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human MSH5 (transcript variant 3) 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: MSH5 (MutS Homolog 5 (MSH5))

Autre désignation: Msh5 (MSH5 Produits)

Synonymes: MSH5 Protein, G7 Protein, MUTSH5 Protein, NG23 Protein, Mut5 Protein, mutS homolog 5 Protein, mutS protein homolog 5 Protein, MSH (MutS Homolog) family Protein, MSH5 Protein, msh5 Protein, LOC100635155 Protein, Msh5 Protein, msh-5 Protein

Sujet: This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms hetero-oligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene.

Poids moléculaire: 92.7 kDa

NCBI Accession: NP_002432

Pathways: M Phase