PUS7L antibody (AA 165-699) (Biotin)
Quick Overview for PUS7L antibody (AA 165-699) (Biotin) (ABIN8028846)
Target
Reactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 165-699
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Purpose
- Anti-PUS7L Antibody Biotin Conjugated
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Cross-Reactivity (Details)
- No cross-reactivity with other proteins
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Purification
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human PUS7L recombinant protein (Position: R165-H699).
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Isotype
- IgG
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Application Notes
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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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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Storage
- -20 °C
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Storage Comment
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
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Expiry Date
- 12 months
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- PUS7L (Pseudouridylate Synthase 7 Homolog-Like (PUS7L))
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Alternative Name
- PUS7L
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Background
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Background: Pseudouridylate synthase 7 homolog-like protein is an enzyme that in humans is encoded by the PUS7L gene. PUS7L (pseudouridylate synthase 7 homolog (S. cerevisiae) -like) is a 701 amino acid protein that belongs to the pseudouridine synthase truD family and contains one TRUD domain. The PUS7L gene is conserved in chimpanzee, canine, bovine, mouse, chicken and zebrafish, and maps to human chromosome 12q12. Encoding over 1,100 genes within 132 million bases, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Noonan syndrome, which includes heart and facial developmental defects among the primary symptoms, is caused by a mutant form of PTPN11 gene product, SH-PTP2. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction.
Gene Full Name: pseudouridine synthase 7 like
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Gene ID
- 83448
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UniProt
- Q9H0K6
Target
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