Thermo Fisher Scientific RUNDC2A Monoclonal Antibody (6D6)

Applications

Tested Dilution

Publications

Western Blot (WB)

1-5 µg/mL

-

Immunocytochemistry (ICC/IF)

10 µg/mL

-

ELISA (ELISA)

10 µg/mL

-

Product Specifications

Species Reactivity

Human, Mouse

Host/Isotype

Mouse / IgG1, kappa

Class

Monoclonal

Type

Antibody

Clone

6D6

Immunogen

RUNDC2A (AAH41583, 1 a.a. approximately 249 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:SNX29,uniProtId:Q8TEQ0-1,ncbiNodeId:9606,antigenRange:1-813,antigenLength:813,antigenImageFileName:H00084127-M02_SNX29_Q8TEQ0-1_House_mouse.svg,antigenImageFileNamePDP:H00084127-M02_SNX29_Q8TEQ0-1_House_mouse_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

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Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

See Label

Purification

Affinity chromatography

Storage buffer

PBS, pH 7.4

Contains

no preservative

Storage conditions

-20° C, Avoid Freeze/Thaw Cycles

Shipping conditions

Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows: MDEERSSMLP TMAAGPNSIL FAINIDNKDL NGQSKFAPTV SDLLKESTQN VTLLKESTQG VSSVFREITA SSAISILIKP EQETDPLPVV SRNVSADAKC KKERKKKKQV TNIISFDDEE DEQNSGDMFK KTPGAGESSE DNSDHSSVNI MSAFESPFGP NSNGSQSSNS WKIDSLSLNR EFGYQKLDVK SIDDEDVDEN EDDVYGNSSG RKHRGHSESP EKNGAHSVTQ AGVQWHDLGS LQPLPPGFR

Target Information

SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn`s disease, which is a gastrointestinal inflammatory condition.

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