EIF4H Rabbit pAb
Sizes: 20µl, 100µl
Catalogue Numbers: A9953-20, A9953-100
Citations, Manuals and SDS Available upon request.
Background: 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.
Synonyms: WSCR1; WBSCR1; eIF-4H; EIF4H
GeneID: 7458
Swiss-Prot: Q15056
Reactivity: Human, Mouse
Calculated Molecular Weight: 27kDa
Observed Molecular Weight: 27kDa
Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-228 of human EIF4H (NP_114381.1).
Immunogen Species: Human
Host: Rabbit
Isotype: IgG
Purity: Affinity purification
Tested Applications: ELISA, WB
Storage Buffer: Store at -20℃. Avoid freeze / thaw cycles. | Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Recommended Dilutions: WB: 1:500 - 1:2000
Research Areas: Epigenetics Nuclear Signaling, RNA Binding
Modifications: Unmodified
Conjugate: Unconjugated
Positive Samples: SH-SY5Y, Jurkat, HeLa, SW480, Mouse pancreas
Cellular Location: Cytoplasm, Perinuclear Region
Category: Polyclonal Antibodies
Citations, Manuals and SDS Available upon request.