Invitrogen™ SNX29 Monoclonal Antibody (6D6)

Mouse Monoclonal Antibody

Supplier:  Invitrogen™ MA522730

Catalog No. PIMA522730

Description

Peptide Sequence: 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.

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.

Specifications

• Antigen: SNX29
• Classification: Monoclonal
• Concentration: 0.2 mg/mL
• Formulation: PBS with no preservative; pH 7.4
• Gene Accession No.: Q8TEQ0, Q9D3S3
• Gene Symbols: SNX29
• Immunogen: RUNDC2A (AAH41583, 1 a.a. ~ 249 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
• Quantity: 100 μg
• Primary or Secondary: Primary
• Target Species: Human, Mouse
• Product Type: Antibody
• Isotype: IgG1 κ

• Applications: ELISA, Western Blot, Immunocytochemistry
• Clone: 6D6
• Conjugate: Unconjugated
• Gene: SNX29
• Gene Alias: 4933437K13Rik; A-388D4.1; ENSMUSG00000079738; Gm11170; Gm1737; Gm930; RUN domain containing 2A; RUN domain-containing protein 2A; RUNDC2A; SNX29; SODD; sorting nexin 29; sorting nexin-29
• Host Species: Mouse
• Purification Method: Affinity Chromatography
• Regulatory Status: RUO
• Gene ID (Entrez): 74478, 92017
• Content And Storage: -20°C, Avoid Freeze/Thaw Cycles
• Form: Liquid