MON1A antibody (Internal Region)
Quick Overview for MON1A antibody (Internal Region) (ABIN498066)
Target
See all MON1A AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 589-601, Internal Region
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Sequence
- C-RPLKTIYYTG PNE
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Specificity
- This antibody is expected to recognize isoforms a and b (NP_115731.2, NP_001135973.1).
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Cross-Reactivity (Details)
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Species reactivity (expected):Mouse, Rat, Canine (Dog), Bovine.
Species reactivity (tested):Human. -
Purification
- Ammonium Sulphate Precipitation followed by Antigen Affinity Chromatography using the immunizing peptide.
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Immunogen
- Peptide with sequence from the internal region of the protein sequence according to NP_115731.2, NP_001135973.1. Genename: MON1A
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Application Notes
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Peptide ELISA: Detection Limit: 1/8000. Western blot: 1-3 μg/mL. Detects a band of Approx 50 kDa in lysates of cell line Jurkat.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. -
Restrictions
- For Research Use only
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Concentration
- 0.5 mg/mL
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Buffer
- Tris saline, pH 7.3 containing 0.02 % Sodium Azide as preservative and 0.5 % BSA as stabilizer
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Preservative
- Sodium azide
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Precaution of Use
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- Avoid repeated freezing and thawing.
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Storage
- 4 °C/-20 °C
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Storage Comment
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- MON1A (MON1 Homolog A (MON1A))
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Alternative Name
- MON1A
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Background
- MON1A also known as SAND1, is a 555 amino acid protein that exists as multiple alternatively spliced isoforms and plays an important role in membrane trafficking, specifically through the secretory apparatus. The gene encoding MON1A maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene clusterand a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. 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.Synonyms: SAND1, Vacuolar fusion protein MON1 homolog A
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Gene ID
- 84315
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NCBI Accession
- NP_001135973
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UniProt
- Q86VX9
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Pathways
- Transition Metal Ion Homeostasis
Target
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