LRRC8A anticorps (AA 760-810)
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- Antigène Voir toutes LRRC8A Anticorps
- LRRC8A (Leucine Rich Repeat Containing 8 Family, Member A (LRRC8A))
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Épitope
- AA 760-810
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Reactivité
- Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp LRRC8A est non-conjugé
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Application
- Western Blotting (WB), Immunoprecipitation (IP)
- Fonction
- Rabbit anti-LRRC8A Antibody, Affinity Purified
- Homologie
- Rat
- Purification
- Affinity Purified
- Immunogène
- Between AA 760 and 810
- Isotype
- IgG
- Top Product
- Discover our top product LRRC8A Anticorps primaire
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- Indications d'application
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IP: 2 - 10 μg/mg lysate
WB: 1:1,000 - 1:5,000
- Restrictions
- For Research Use only
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- Concentration
- 1000 μg/mL
- Buffer
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C
- Date de péremption
- 12 months
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- Antigène
- LRRC8A (Leucine Rich Repeat Containing 8 Family, Member A (LRRC8A))
- Autre désignation
- LRRC8A (LRRC8A Produits)
- Synonymes
- anticorps AGM5, anticorps LRRC8, anticorps Lrrc8, anticorps mKIAA1437, anticorps wu:fb18g12, anticorps wu:fi21b10, anticorps LLRC8A, anticorps leucine rich repeat containing 8 VRAC subunit A, anticorps leucine rich repeat containing 8A, anticorps leucine rich repeat containing 8 VRAC subunit Aa, anticorps leucine-rich repeat containing 8 family member A S homeolog, anticorps leucine rich repeat containing 8 family member A, anticorps LRRC8A, anticorps Lrrc8a, anticorps lrrc8aa, anticorps lrrc8a.S
- Sujet
- Background: LRRC8A belongs to the leucine-rich repeat family of proteins, which are involved in diverse biological processes, including cell adhesion, cellular trafficking, and hormone-receptor interactions. LRRC8A is a putative four-pass transmembrane protein that plays a role in B cell development. Defects in the LRRC8A gene cause autosomal dominant non-Bruton type agammaglobulinemia, an immunodeficiency disease resulting from defects in B cell maturation [taken from NCBI Entrez Gene (Gene ID: 56262)].
- ID gène
- 56262
- NCBI Accession
- NP_001120716
- UniProt
- Q8IWT6
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