Thermo Fisher Scientific MOB3A/MOB3B Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

1:500-1:1,000

-

Immunocytochemistry (ICC/IF)

1:100-1:500

-

Product Specifications

Species Reactivity

Human, Mouse

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

A synthesized peptide derived from human MOB3A(Accession Q96BX8), corresponding to amino acid residues M1-N40. if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:MOB3A/MOB3B,uniProtId:Q96BX8-1,ncbiNodeId:9606,antigenRange:1|1-40,antigenLength:217,antigenImageFileName:PA5-101233_MOB3AMOB3B_Q96BX8-1_Rabbit.svg,antigenImageFileNamePDP:PA5-101233_MOB3AMOB3B_Q96BX8-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

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Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1 mg/mL

Purification

Affinity chromatography

Storage buffer

PBS, pH 7.4, with 50% glycerol

Contains

0.02% sodium azide

Storage conditions

-20°C

Shipping conditions

Wet ice

RRID

AB_2850674

Product Specific Information

Antibody detects endogenous levels of total MOBKL2A/B.

Target Information

MOBKL2A (Mps one binder kinase activator-like 2A), also known as MOB-LAK or MOB3A, is a 217 amino acid protein that regulates kinase activity. A member of the MOB1/phocein family, MOBKL2A is encoded by a gene that maps to human chromosome 19. Consisting of around 63 million bases with over 1,400 genes, chromosome 19 makes up over 2% of human genomic DNA. Chromosome 19 includes a diversity of interesting genes and is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG family, and Fcα receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.