SCCPDH antibody
Quick Overview for SCCPDH antibody (ABIN7260229)
Target
See all SCCPDH AntibodiesReactivity
Host
Clonality
Conjugate
Application
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    - 
                                            Characteristics
- Polyclonal Antibody
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                                            Purification
- Affinity purification
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                                            Immunogen
- Recombinant fusion protein of human SCCPDH (NP_057086.2).
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                                            Isotype
- IgG
 
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                                            Application Notes
- WB 1:500-1:2000
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                                            Restrictions
- For Research Use only
 
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                                            Format
- Liquid
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                                            Concentration
- 1 mg/mL
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                                            Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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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
- Store at -20°C. Avoid freeze / thaw cycles.
 
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    - SCCPDH (Saccharopine Dehydrogenase (SCCPDH))
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                                            Alternative Name
- SCCPDH
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                                            Background
- SCCPDH (Probable saccharopine dehydrogenase) is a 429 amino acid protein that belongs to the saccharopine dehydrogenase family. The SCCPDH gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken, fruit fly, mosquito and C.elegans, and maps to human chromosome 1q44. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
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                                            Molecular Weight
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                        Observed_MW: 45 kDa Calculated_MW: 47 kDa 
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                                            Gene ID
- 51097
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                                            UniProt
- Q8NBX0
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                                            Pathways
- SARS-CoV-2 Protein Interactome
 Target
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