LRRC8A antibody (AA 760-810)
-
- Target See all LRRC8A Antibodies
- LRRC8A (Leucine Rich Repeat Containing 8 Family, Member A (LRRC8A))
-
Binding Specificity
- AA 760-810
-
Reactivity
- Human, Mouse
-
Host
- Rabbit
-
Clonality
- Polyclonal
-
Conjugate
- This LRRC8A antibody is un-conjugated
-
Application
- Western Blotting (WB), Immunoprecipitation (IP)
- Purpose
- Rabbit anti-LRRC8A Antibody, Affinity Purified
- Predicted Reactivity
- Rat
- Purification
- Affinity Purified
- Immunogen
- Between AA 760 and 810
- Isotype
- IgG
- Top Product
- Discover our top product LRRC8A Primary Antibody
-
-
- Application Notes
-
IP: 2 - 10 μg/mg lysate
WB: 1:1,000 - 1:5,000
- Restrictions
- For Research Use only
-
- Concentration
- 1000 μg/mL
- Buffer
- Tris-citrate/phosphate buffer, pH 7 to 8 containing 0.09 % Sodium Azide
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C
- Expiry Date
- 12 months
-
- Target
- LRRC8A (Leucine Rich Repeat Containing 8 Family, Member A (LRRC8A))
- Alternative Name
- LRRC8A (LRRC8A Products)
- Synonyms
- AGM5 antibody, LRRC8 antibody, Lrrc8 antibody, mKIAA1437 antibody, wu:fb18g12 antibody, wu:fi21b10 antibody, LLRC8A antibody, leucine rich repeat containing 8 VRAC subunit A antibody, leucine rich repeat containing 8A antibody, leucine rich repeat containing 8 VRAC subunit Aa antibody, leucine-rich repeat containing 8 family member A S homeolog antibody, leucine rich repeat containing 8 family member A antibody, LRRC8A antibody, Lrrc8a antibody, lrrc8aa antibody, lrrc8a.S antibody
- Background
- 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)].
- Gene ID
- 56262
- NCBI Accession
- NP_001120716
- UniProt
- Q8IWT6
-