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EIF4H Antibody immunohistochemistry analysis in formalin fixed and paraffin embedded human pancreas tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.
Western blot analysis in MDA-MB231,Hela cell line lysates (35ug/lane).
EIF4H Antibody immunohistochemistry analysis in formalin fixed and paraffin embedded human pancreas tissue followed by peroxidase conjugation of the secondary antibody and DAB staining.

EIF4H Antibody

CATALOG NUMBER: 56-537

Clonality:
Polyclonal
Tested Applications:
IHC-P, WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Homology:
Predicted species reactivity based on immunogen sequence: Mouse
Immunogen:
This EIF4H antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 127-156 amino acids from the Central region of human EIF4H.
Conjugate:
Unconjugated
Tested Applications:
IHC-P, WB
Application Note:
For IHC-P starting dilution is: 1:10~50
For WB starting dilution is: 1:1000
Predicted Molecular Weight:
27 kDa
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality:
Polyclonal
Isotype:
Rabbit Ig
Physical State:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Storage Conditions:
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Ncbi Official Symbol:
EIF4H
Additional Names:
Eukaryotic translation initiation factor 4H, eIF-4H, Williams-Beuren syndrome chromosomal region 1 protein, EIF4H, KIAA0038, WBSCR1, WSCR1
Protein Accession Number:
Q15056
Protein Gi Number:
18276665
Ncbi Gene Id Number:
7458
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
This gene encodes one of the translation initiationfactors, which functions to stimulate the initiation of proteinsynthesis at the level of mRNA utilization. This gene is deleted inWilliams syndrome, a multisystem developmental disorder caused bythe deletion of contiguous genes at 7q11.23. Alternative splicingof this gene generates 2 transcript variants.
Background Reference 1:
Feng, T., et al. Hum. Genet. 128(3):269-280(2010)
Background Reference 2:
Zhu, X., et al. Genet. Epidemiol. 34(2):171-187(2010)
Background Reference 3:
Mokas, S., et al. Mol. Biol. Cell 20(11):2673-2683(2009)
Background Reference 4:
Marintchev, A., et al. Cell 136(3):447-460(2009)

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

56-537

List Size:
400 ul

List Price:

$495.00

Datasheet
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