GeneBio Systems
Anti-RPS4/X/Y1/Y2 Antibody Picoband®
Anti-RPS4/X/Y1/Y2 Antibody Picoband®
SKU:A09096-1
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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,Flow Cytometry,ELISA
Application Details: Western blot, 0.1-0.25 μg/ml, Human, Moue, Rat
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/ml, -
Gene Name: RPS4/X/Y1/Y2
Specificity:
Background: 40S ribosomal protein S4, X isoform is a protein that in humans is encoded by the RPS4X gene. Cytoplasmic ribosomes, organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes ribosomal protein S4, a component of the 40S subunit. Ribosomal protein S4 is the only ribosomal protein known to be encoded by more than one gene, namely this gene and ribosomal protein S4, Y-linked (RPS4Y). The 2 isoforms encoded by these genes are not identical, but are functionally equivalent. Ribosomal protein S4 belongs to the S4E family of ribosomal proteins. This gene is not subject to X-inactivation. It has been suggested that haploinsufficiency of the ribosomal protein S4 genes plays a role in Turner syndrome; however, this hypothesis is controversial. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome.
Immunogen: E.coli-derived human RPS4/X/Y1/Y2 recombinant protein (Position: M1-G263).
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. Fisher, E. M. C., Beer-Romero, P., Brown, L. G., Ridley, A., McNeil, J. A., Lawrence, J. B., Willard, H. F., Bieber, F. R., Page, D. C. Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome. Cell 63: 1205-1218, 1990. 2. Geerkens, C., Just, W., Held, K. R., Vogel, W. Ullrich-Turner syndrome is not caused by haploinsufficiency of RPS4X. Hum. Genet. 97: 39-44, 1996. 3. Hamvas, R. M., Brown, S. D., Keer, J. T., Fisher, E. M., Romero, P., Zinn, A., Page, D. The mapping of the locus Rps4 to the X-inactivation region in the mouse. (Abstract) Cytogenet. Cell Genet. 58: 2065-2066, 1991.
Uniprot ID: P62701/RPS4Y1/Q8TD47
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: 30 kDa
Calculated Molecular Weight:
Gene ID: 6191/6192/140032
Protein Name: DNA repair protein RAD51 homolog
Gene Full Name: tudor domain containing 3
Synonyms: RPS4X; CCG2; RPS4; SCAR; 40S ribosomal protein S4, X isoform; SCR10; Single copy abundant mRNA protein; Small ribosomal subunit protein eS4; RPS4Y1; RPS4Y; PRO2646; 40S ribosomal protein S4, Y isoform 1; RPS4Y2; RPS4Y2P; 40S ribosomal protein S4, Y isoform 2
