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WBSCR1 Monoclonal Antibody (4B2)

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Datasheet
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Datasheet
Protocols
Questions & Answers

Cite WBSCR1 Monoclonal Antibody (4B2)

  • Antibody Testing Data (1)
WBSCR1 Antibody in Western Blot (WB)
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WBSCR1 Antibody in Western Blot (WB)
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WBSCR1 Antibody (H00007458-M07) in WB

Western Blot analysis of WBSCR1 expression in transfected 293T cell line by WBSCR1 monoclonal antibody (M07), clone 4B2. Lane 1: WBSCR1 transfected lysate(27.4 KDa). Lane 2: Non-transfected lysate. . {{ $ctrl.currentElement.advancedVerification.fullName }} validation info. View more
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WBSCR1 Antibody in Western Blot (WB)
WBSCR1 Monoclonal Antibody (4B2)

Product Details

H00007458-M07

Applications
Tested Dilution
Publications

Western Blot (WB)

1-5 µg/mL
-

ELISA (ELISA)

10 µg/mL
-
Product Specifications

Species Reactivity

Human

Host/Isotype

Mouse / IgG2a, kappa

Class

Monoclonal

Type

Antibody

Clone

4B2

Immunogen

WBSCR1 (NP_114381.1, 1 a.a. approximately 100 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
View immunogen

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

Protein A

Storage buffer

PBS, pH 7.4

Contains

no preservative

Storage conditions

-20°C, Avoid Freeze/Thaw Cycles

Shipping conditions

Wet ice

Product Specific Information

Product may be used with Western Blot (Transfected lysate).

Immunogen sequence: MADFDTYDDR AYSSFGGGRG SRGSAGGHGS RSQKELPTEP PYTAYVGNLP FNTVQGDIDA IFKDLSIRSV RLVRDKDTDK FKGFCYVEFD EVDSLKEALT

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 chromosome region 1

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Gene Aliases: eIF-4H; EIF4H; KIAA0038; WBSCR1; WSCR1

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UniProt ID: (Human) Q15056

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Entrez Gene ID: (Human) 7458

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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
Process(es)
formation of translation preinitiation complex cytoplasmic translation translational initiation regulation of translational initiation viral process sexual reproduction developmental growth 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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