Gnb1l Antibodies

AND Gnb1l ELISA kits, Gnb1l Proteins

Many biological assays use antibodies to detect Gnb1l, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Gnb1l in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Gnb1l antibodies...

We validate the specificity of these antibodies to Gnb1l by testing them on tissues known to express Gnb1l positively and negatively. Browse below to find the Gnb1l antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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Gnb1l Infographic by Boster Bio

All Gnb1l Products

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Product

Figures

Specificity

Applications

Price

Anti-GNB1L Antibody

Human, Mouse, Rat

$405
Cat # A11797
100ul

GNB1L (NM_053004) Human Over-expression Lysate

Human

$628
Cat # LS054584
100 µg

Gnb1l Overview

Facts about Guanine nucleotide-binding protein subunit beta-like protein 1.

Guanine nucleotide-binding protein subunit beta-like protein 1 (Gnb1l)

Gene Information

Mouse
Gene Name:	Gnb1l
Uniprot:	Q9EQ15
Entrez:	13972

Family

Belongs to:

No superfamily

Alternative Names

DGCRK3; G-protein beta subunit-like protein; guanine nucleotide binding protein (G protein), beta polypeptide 1-like; guanine nucleotide binding protein beta-subunit-like polypeptide; guanine nucleotide-binding protein subunit beta-like protein 1; GY2WD40 repeat-containing protein deleted in VCFS; KIAA1645; WD repeat-containing protein 14; WDR14G protein subunit beta-like protein 1; WDVCF

Molecular Weight

Mass (kDA):
35.663 kDA

Genomic Context


Mouse

Location:	16 A3\|16 11.46 cM
Sequence:	16;

Tissue Specificity

Expressed at low levels in most tissues and highly expressed in adult testis.

Diseases

Schizophrenia
Digeorge Syndrome
Haploinsufficiency
22q11 Deletion Syndrome
Mental Disorders
Congenital Heart Disease
Bipolar Disorder
Congenital Abnormality
Psychotic Disorders
Heart Diseases
Monosomy
Circling Gait
Otitis Media Chronic

Otitis Media
Aneuploidy
Carcinoma
Dysplasia
Cat Eye Syndrome
Diseases In Twins
Ventricular Septal Defects

Pathways

Prepulse Inhibition
Regeneration
Ventricular Septum Development
Cell Death
Liver Regeneration
Pathogenesis

Localization

Research Areas

Signal Transduction

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Gnb1l

References

PMID: 11350118 by Funke B., et al. Isolation and characterization of a novel gene containing WD40 repeats from the region deleted in velo-cardio-facial/DiGeorge syndrome on chromosome 22q11.