Eukaryotic Translation Initiation Factor 4H (EIF4H) Antibody
292.5€ (80 µl)
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
935106861
info@markelab.com
name
Eukaryotic Translation Initiation Factor 4H (EIF4H) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx026917
tested applications
ELISA, WB, IHC
Description
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Eukaryotic Translation Initiation Factor 4H (EIF4H) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | WB: 1/1000, IHC-P: 1/10 - 1/50. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified through a protein A column, followed by peptide affinity purification. |
| Size 1 | 80 µl |
| Size 2 | 400 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC |
| Buffer | PBS containing 0.09% sodium azide. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q15056 |
| Background | Antibody anti-EIF4H |
| Status | RUO |
Descripción
Related Products
EIF4H antibody
Stimulates the RNA helicase activity of EIF4A in the translation initiation complex. Binds weakly mRNA.
Ver Producto
Eukaryotic Translation Initiation Factor 4H (EIF4H) Antibody
This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.
Ver Producto
Eukaryotic Translation Initiation Factor 4H (EIF4H) Antibody
Rabbit Polyclonal against the EIF4H protein.
Ver Producto