LRRC8A Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)
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- Target Alle LRRC8A Proteine anzeigen
- LRRC8A (Leucine Rich Repeat Containing 8 Family, Member A (LRRC8A))
- Protein-Typ
- Recombinant
- Proteineigenschaft
- Transcript Variant 3
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Spezies
- Human
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Quelle
- HEK-293 Cells
- Aufreinigungstag / Konjugat
- Dieses LRRC8A Protein ist gelabelt mit Myc-DYKDDDDK Tag.
- Applikation
- Antibody Production (AbP), Standard (STD)
- Produktmerkmale
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- Recombinant human LRRC8A (transcript variant 3) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Reinheit
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product LRRC8A Protein
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- Applikationshinweise
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Kommentare
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The tag is located at the C-terminal.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- 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.
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- 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_001120717
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