SH3BGR Antibodies

AND SH3BGR ELISA kits, SH3BGR Proteins

Many biological assays use antibodies to detect SH3BGR, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with SH3BGR in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop SH3BGR antibodies...

We validate the specificity of these antibodies to SH3BGR by testing them on tissues known to express SH3BGR positively and negatively. Browse below to find the SH3BGR antibody that suites your experiment. We have 3 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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SH3BGR Infographic by Boster Bio

All SH3BGR Products

Product

Figures

Specificity

Applications

Price

Anti-SH3BGR Antibody

1 Q&As

Human, Mouse, Rat

ELISA, WB

$335
Cat # A13419
100ul

Anti-SH3BGR Mouse Monoclonal Antibody [Clone ID: OTI4G5]

Human

IHC, WB

$523
Cat # M13419
100 µl

SH3BGR (NM_007341) Human Over-expression Lysate

Human

$628
Cat # LS006450
100 µg

SH3BGR Overview

Facts about SH3 domain-binding glutamic acid-rich protein.

SH3BGR 3D structure. Source: alphafold

SH3 domain-binding glutamic acid-rich protein (SH3BGR)

Gene Information

Human
Gene Name:	SH3BGR
Uniprot:	P55822
Entrez:	6450

Family

Belongs to:

SH3BGR family

Alternative Names

21-GARP21-glutamic acid-rich protein; 21-Glutamic Acid-Rich Protein (21-GARP)10SH3-binding domain and glutamic acid-rich protein; SH3 domain binding glutamic acid-rich protein; SH3 domain-binding glutamic acid-rich protein; SH3BGR protein; SH3GBR

Molecular Weight

Mass (kDA):
26.086 kDA

Genomic Context


Human

Location:	21q22.2
Sequence:	21; NC_000021.9 (39445865..39515506)

Tissue Specificity

Expressed in heart and skeletal muscle.

Diseases

Down Syndrome
Heart Diseases
Congenital Heart Disease
Congenital Heart Defects
Congenital Abnormality
Muscle Hypotonia
Trisomy
Dysequilibrium Syndrome
Cell Transformation, Neoplastic
Tissue Adhesions
Common Atrioventricular Canal
Congenital Disorders

Heart Septal Defects
Neoplasms
Nervousness
Acute Promyelocytic Leukemia
Leukemia
Steroid Sulfatase Deficiency Disease
Atrioventricular Septal Defect And Common Atrioventricular Junction

Pathways

Pathogenesis
Heart Morphogenesis
Transport
Ras Protein Signal Transduction
Cell Adhesion
Positive Regulation Of Fat Cell Differentiation
System Development
Fatty Acid Transport
Cell Cycle
Regulation Of Fat Cell Differentiation
Regulation Of Mitosis
Cell Differentiation
Lipid Transport

Visual Perception
Circadian Rhythm
Establishment Of Blood-nerve Barrier
Mitosis
Protein Transport
Wnt Receptor Signaling Pathway
Dna Replication

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/SH3BGR

References

PMID: 9050928 by Scartezzini P., et al. Cloning a new human gene from chromosome 21q22.3 encoding a glutamic acid-rich protein expressed in heart and skeletal muscle.