MID2 Antibodies

AND MID2 ELISA kits, MID2 Proteins

Many biological assays use antibodies to detect MID2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with MID2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop MID2 antibodies...

We validate the specificity of these antibodies to MID2 by testing them on tissues known to express MID2 positively and negatively. Browse below to find the MID2 antibody that suites your experiment. We have 1 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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MID2 Infographic by Boster Bio

All MID2 Products

Product

Figures

Specificity

Applications

Price

MID2 (NM_052817) Human Over-expression Lysate

Human

$628
Cat # LS011043
100 µg

MID2 Overview

Facts about Probable E3 ubiquitin-protein ligase MID2.

MID2 3D structure. Source: alphafold

Probable E3 ubiquitin-protein ligase MID2 (MID2)

May play a role in microtubule stabilization. .

Gene Information

Human
Gene Name:	MID2
Uniprot:	Q9UJV3
Entrez:	11043

Family

Belongs to:

TRIM/RBCC family

Alternative Names

EC 6.3.2.-; FLJ37715; FLJ41813; FXY2midin-2; midin 2; Midin-2; midline 2; Midline defect 2; Midline-2; RING finger protein 60; RNF60midline-2; TRIM1probable E3 ubiquitin-protein ligase MID2; tripartite motif protein 1; Tripartite motif-containing protein 1

Molecular Weight

Mass (kDA):
83.21 kDA

Genomic Context


Human

Location:	Xq22.3
Sequence:	X; NC_000023.11 (107820453..107931637)

Tissue Specificity

Low level in fetal kidney and lung, and in adult prostate, ovary and small intestine.

Subcellular Localizations

Cytoplasm. Cytoplasm, cytoskeleton. Microtubule-associated.

Diseases

Smith-lemli-opitz Syndrome
Opitz-g Syndrome, Type 2
Physiological Stress
Stenosis
Orbital Separation Excessive
Fg Syndrome
Cell Transformation, Neoplastic
Congenital Abnormality
Genetic Diseases, X-linked
Hypospadias
Tuberculosis, Pulmonary
Arteriovenous Malformation

Sex Chromosome Disorders
Hermaphroditism
Malignant Neoplasms
Abdominal Colic
Chimera Disorder
Cleft Lip

Pathways

Localization
Cell Cycle
Cytokinesis
Transport
Hypersensitivity
Mating
Anaphase
Cell Division
Secretory Pathway
Septin Ring Disassembly
Cytoskeleton Organization
Exocytosis
Actin Cytoskeleton Organization

Mitosis
Endocytosis
Mapk Cascade
Cell Growth
Pathogenesis
Secretion
Response To Pheromone

PTMs

Phosphorylation
Glycosylation

Dephosphorylation
Cleavage

Research Areas

Zinc Finger

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/MID2

References

PMID: 10644436 by Perry J., et al. FXY2/MID2, a gene related to the X-linked Opitz syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules.

PMID: 10400986 by Buchner G., et al. MID2, a homologue of the Opitz syndrome gene MID1: similarities in a sub-cellular localization and differences in expression during development.