ABIN1002684
antibody from antibodies-online
Targeting: NLRC4
CARD12, CLAN, CLAN1, CLANA, CLANB, CLANC, CLAND, CLR2.1, ipaf
Antibody data
- Antibody Data
- Antigen structure
- References [3]
- Comments [0]
- Validations [0]
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- Product number
- ABIN1002684 - Provider product page
- Provider
- antibodies-online
- Product name
- anti-NLR Family, CARD Domain Containing 4 (NLRC4) antibody
- Antibody type
- Polyclonal
- Antigen
- Rabbit polyclol ARTS antibody was raised against a synthetic peptide corresponding to amino acids near the amino terminus of human ARTS (GenBank accession number NP_536540).
- Description
- Affinity chromatography purified via peptide column.
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 μg
- Storage
- 4°C
- Handling
- Antibody can be stored at 4ºC, stable for one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures. During shipment, small volumes of antibody will occasionally become entrapped in the seal of the product vial. For products with volumes of 200 myl or less, we recommend gently tapping the vial on a hard surface or briefly centrifuging the vial in a tabletop centrifuge to dislodge any liquid in the container?s cap.
Submitted references A novel mitochondrial septin-like protein, ARTS, mediates apoptosis dependent on its P-loop motif.
Characterization and expression analysis of two human septin genes, PNUTL1 and PNUTL2.
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene.
Larisch S, Yi Y, Lotan R, Kerner H, Eimerl S, Tony Parks W, Gottfried Y, Birkey Reffey S, de Caestecker MP, Danielpour D, Book-Melamed N, Timberg R, Duckett CS, Lechleider RJ, Steller H, Orly J, Kim SJ, Roberts AB
Nature cell biology 2000 Dec;2(12):915-21
Nature cell biology 2000 Dec;2(12):915-21
Characterization and expression analysis of two human septin genes, PNUTL1 and PNUTL2.
Zieger B, Tran H, Hainmann I, Wunderle D, Zgaga-Griesz A, Blaser S, Ware J
Gene 2000 Dec 31;261(2):197-203
Gene 2000 Dec 31;261(2):197-203
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene.
Paavola P, Horelli-Kuitunen N, Palotie A, Peltonen L
Genomics 1999 Jan 1;55(1):122-5
Genomics 1999 Jan 1;55(1):122-5
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