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  • eIF4H Antibodies

Bioss

eIF4H Polyclonal Antibody

View all (11) eIF4H antibodies

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Datasheet
Protocols
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Datasheet
Protocols
Questions & Answers

Cite eIF4H Polyclonal Antibody

  • Antibody Testing Data (2)
eIF4H Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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eIF4H Antibody in Immunohistochemistry (Paraffin) (IHC (P))
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FIGURE: 1 / 2

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eIF4H Antibody (BS-14553R) in IHC (P)

Formalin-fixed and paraffin embedded human laryngeal tissue labeled with Rabbit Anti-eIF4H Polyclonal Antibody, Unconjugated (bs-14553R) at 1:200 followed by conjugation to the secondary antibody and DAB staining. {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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eIF4H Antibody in Immunohistochemistry (Paraffin) (IHC (P))
eIF4H Antibody in Immunohistochemistry (Paraffin) (IHC (P))
eIF4H Polyclonal Antibody

Product Details

BS-14553R

Applications
Tested Dilution
Publications

Immunohistochemistry (Paraffin) (IHC (P))

1:200
-

Immunohistochemistry (Frozen) (IHC (F))

1:100-1:500
-

Immunocytochemistry (ICC/IF)

1:100-1:500
-

ELISA (ELISA)

1:500-1:1,000
-
Product Specifications

Species Reactivity

Human, Mouse, Rat

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

KLH conjugated synthetic peptide derived from human eIF4H, amino acids 31-130.
View immunogen

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

Protein A

Storage buffer

0.01M TBS, pH 7.4, with 50% glycerol, 1% BSA

Contains

0.02% ProClin 300

Storage conditions

-20°C

Shipping conditions

Ambient (domestic); Wet ice (international)

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, (Rat) Q5XI72

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Entrez Gene ID: (Human) 7458, (Mouse) 22384, (Rat) 288599

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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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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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