GeneBio Systems
Anti-UBA5 Antibody Picoband®
Anti-UBA5 Antibody Picoband®
SKU:A06385-2
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Size: 100 μg
Storage: At -20℃ for one year from date of receipt. After reconstitution, at 4℃ for one month. It can also be aliquotted and stored frozen at -20℃ for six months. Avoid repeated freezing and thawing.
Form: Lyophilized
Reactivity: Human,Mouse,Rat
Applications: WB,IHC,IP,Flow Cytometry,ELISA
Application Details: Western blot, 0.1-0.25 μg/ml, Human, Mouse, Rat
Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/ml, Human
Immunoprecipitation, 0.5-2 μg/ml, Human
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/ml, -
Gene Name: UBA5
Specificity:
Background: Ubiquitin-like modifier-activating enzyme 5 is a protein that in humans is encoded by the UBA5 gene. This gene encodes a member of the E1-like ubiquitin-activating enzyme family. This protein activates ubiquitin-fold modifier 1, a ubiquitin-like post-translational modifier protein, via the formation of a high-energy thioester bond. Alternative splicing results in multiple transcript variants. A pseudogene of this gene has been identified on chromosome 1.
Immunogen: E.coli-derived human UBA5 recombinant protein (Position: R37-D389).
Clonality: Polyclonal
Contents: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
Purification: Immunogen affinity purified.
Reconstitution: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Reference: 1. Colin, E., Daniel, J., Ziegler, A., Wakim, J., Scrivo, A., Haack, T. B., Khiati, S., Denomme, A.-S., Amati-Bonneau, P., Charif, M., Procaccio, V., Reynier, P., and 19 others. Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy. Am. J. Hum. Genet. 99: 695-703, 2016. 2. Dou, T., Gu, S., Liu, J., Chen, F., Zeng, L., Guo, L., Xie, Y., Mao, Y. Isolation and characterization of ubiquitin-activating enzyme E1-domain containing 1, UBE1DC1. Molec. Biol. Rep. 32: 265-271, 2005. 3. Duan, R., Shi, Y., Yu, L., Zhang, G., Li, J., Lin, Y., Guo, J., Wang, J., Shen, L., Jiang, H., Wang, G., Tang, B. UBA5 mutations cause a new form of autosomal recessive cerebellar ataxia. PLoS One 11: e0149039, 2016. Note: Electronic Article.
Uniprot ID: Q9GZZ9
Host: Rabbit
Concentration: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
Conjugate:
Cross Reactivity: No cross-reactivity with other proteins.
Isotype: Rabbit IgG
Phospho_site:
Clone Number:
Observed Molecular Weight: 50 kDa
Calculated Molecular Weight: 26056 MW
Gene ID: 79876
Protein Name: Ubiquitin-like modifier-activating enzyme 5
Gene Full Name: ubiquitin like modifier activating enzyme 5
Synonyms: FLJ23251UBA5; THIFP1; UBA5; UBE1DC1; Ubiquitin activating enzyme 5; UFM1 activating enzyme
