LRRC33 antibody (AA 501-600) (AbBy Fluor® 647)
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- Target See all LRRC33 (NRROS) Antibodies
- LRRC33 (NRROS) (Negative Regulator of Reactive Oxygen Species (NRROS))
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Binding Specificity
- AA 501-600
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Reactivity
- Human, Rat, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This LRRC33 antibody is conjugated to AbBy Fluor® 647
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Application
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Cross-Reactivity
- Human, Mouse, Rat
- Predicted Reactivity
- Rabbit
- Purification
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human LRRC33
- Isotype
- IgG
- Top Product
- Discover our top product NRROS Primary Antibody
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- Application Notes
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Preservative
- ProClin
- Precaution of Use
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Expiry Date
- 12 months
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- Target
- LRRC33 (NRROS) (Negative Regulator of Reactive Oxygen Species (NRROS))
- Alternative Name
- LRRC33 (NRROS Products)
- Synonyms
- GARPL1 antibody, LRRC33 antibody, UNQ3030 antibody, negative regulator of reactive oxygen species antibody, NRROS antibody
- Background
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Synonyms: ELLP3030, GARPL1, NRROS_HUMAN, Leucine rich repeat containing protein 33, Lrcc33, UNQ3030.
Background: LRRC33 is a 692 amino acid protein that contains 17 LRR repeats. The gene encoding LRRC33 maps to chromosome 3, which encodes over 1,100 genes. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Marfan syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.
- Gene ID
- 375387
- UniProt
- Q86YC3
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