LRRC8A Protein (Transcript Variant 2) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2724946

Produktdetails

Target: LRRC8A (Leucine Rich Repeat Containing 8 Family, Member A (LRRC8A))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 2

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses LRRC8A Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

• Recombinant human LRRC8A (transcript variant 2) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

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

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: 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.

Antigendetails

Target: LRRC8A (Leucine Rich Repeat Containing 8 Family, Member A (LRRC8A))

Andere Bezeichnung: Lrrc8a (LRRC8A Produkte)

Synonyme: AGM5 Protein, LRRC8 Protein, Lrrc8 Protein, mKIAA1437 Protein, wu:fb18g12 Protein, wu:fi21b10 Protein, LLRC8A Protein, leucine rich repeat containing 8 VRAC subunit A Protein, leucine rich repeat containing 8A Protein, leucine rich repeat containing 8 VRAC subunit Aa Protein, leucine-rich repeat containing 8 family member A S homeolog Protein, leucine rich repeat containing 8 family member A Protein, LRRC8A Protein, Lrrc8a Protein, lrrc8aa Protein, lrrc8a.S Protein

Hintergrund: This gene encodes a protein belonging to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. This family member is a putative four-pass transmembrane protein that plays a role in B cell development. Defects in this gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene.

Molekulargewicht: 94 kDa

NCBI Accession: NP_062540