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  • Primary Antibodies ›
  • eIF4H Antibodies

Invitrogen

eIF4H Polyclonal Antibody

View all (11) eIF4H antibodies

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Datasheet
Protocols
Questions & Answers
Datasheet
Protocols
Questions & Answers

Cite eIF4H Polyclonal Antibody

  • Antibody Testing Data (3)
eIF4H Antibody in Immunocytochemistry (ICC/IF)
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eIF4H Antibody in Immunocytochemistry (ICC/IF)
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eIF4H Antibody (PA5-115170) in ICC/IF

Immunocytochemistry analysis of eIF4H in A549 cells. Samples were treated with PFA, permeabilized in 0.1% Triton X-100, blocked in 10% serum (45 min at 25°C), and incubated with polyclonal antibody (Product # PA5-115170). Secondary staining was applied with mouse anti-beta tubulin (1 hr at 37°, AlexaFluor 594 conjugated goat anti-rabbit IgG (Red), AlexaFluor 488 conjugated goat anti-mouse IgG (Green) and DAPI. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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eIF4H Antibody in Immunocytochemistry (ICC/IF)
eIF4H Antibody in Western Blot (WB)
eIF4H Antibody in Western Blot (WB)
eIF4H Polyclonal Antibody

Product Details

PA5-115170

Applications
Tested Dilution
Publications

Western Blot (WB)

1:500-1:2,000
-

Immunocytochemistry (ICC/IF)

1:100-1:500
-
Product Specifications

Species Reactivity

Human, Mouse

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

A synthesized peptide derived from human EIF4H(Accession Q15056), corresponding to amino acid residues D8-I58.
View immunogen

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

Affinity chromatography

Storage buffer

PBS with 50% glycerol

Contains

0.02% sodium azide

Storage conditions

-20°C

Shipping conditions

Wet ice

RRID

AB_2899806

Product Specific Information

Antibody detects endogenous levels of total EIF4H.

Target Information

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.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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Bioinformatics

Protein Aliases: eIF-4H; Eukaryotic translation initiation factor 4H; Williams-Beuren syndrome chromosomal region 1 protein; Williams-Beuren syndrome chromosomal region 1 protein homolog; Williams-Beuren syndrome chromosome region 1; Williams-Beuren syndrome chromosome region 1 homolog

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Gene Aliases: AU018978; D5Ertd355e; E430026L18Rik; Ef4h; eIF-4H; EIF4H; KIAA0038; mKIAA0038; WBSCR1; WSCR1

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UniProt ID: (Human) Q15056, (Mouse) Q9WUK2

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Entrez Gene ID: (Human) 7458, (Mouse) 22384

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Function(s)
nucleotide binding RNA binding translation initiation factor activity helicase activity protein binding translation factor activity, RNA binding RNA strand annealing activity RNA strand-exchange activity ribosomal small subunit binding poly(A) RNA binding cadherin binding involved in cell-cell adhesion nucleic acid binding
Process(es)
translation translational initiation sexual reproduction developmental growth formation of translation preinitiation complex cytoplasmic translation regulation of translational initiation viral process eukaryotic translation initiation factor 4F complex assembly cell-cell adhesion
It has to be done as per old AB suggested Products section.
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Performance Guarantee

If an Invitrogen™ antibody doesn't perform as described on our website or datasheet,we'll replace the product at no cost to you, or provide you with a credit for a future purchase.*

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