Anti-CCDC22 antibody produced in rabbit

• Supplier: Sigma-Aldrich
• Catalog: HPA000888
• Prices: $429.00
• Sizes: 100 µl
• Host: Rabbit
• Clonality: Polyclonal
• Applications: IHC-P WB
• Species Reactivities: Rat, Mouse, Human
• Antigen: Coiled-coil domain-containing protein 22 recombinant protein epitope signature tag (PrEST)
• Description: Rabbit Polyclonal
• Gene: CCDC22
• Conjugate: unconjugated

Product images

Immunohistochemistry
Anti-CCDC22: Cat. No. HPA000888: Immunoperoxidase staining of formalin-fixed, paraffin-embedded human stomach tissue showing cytoplasmic staining of parietal cells.

Immunofluorescence
Anti-CCDC22: Cat. No. HPA000888: Immunofluorescent staining of Human cell line U-251MG shows positivity in nucleus but not nucleoli and cytoplasm.

Immunoblotting
Anti-CCDC22: Cat. No. HPA000888:
Lanes
1. Marker [kDa] 219, 112, 85, 49, 32, 25, 18
2. Human cell line RT-4

Immunoblotting
Anti-CCDC22: Cat. No. HPA000888:
Lanes
1. NIH-3T3 cell lysate (Mouse embryonic fibroblast cells)
2. NBT-II cell lysate (Rat Wistar bladder tumour cells)
3. PC12 cell lysate (Pheochromocytoma of rat adrenal medulla)

Product References

COMMD1 is linked to the WASH complex and regulates endosomal trafficking of the - COMMD1 is linked to the WASH complex and regulates endosomal trafficking of the

Phillips-Krawczak CA, Singla A, Starokadomskyy P, Deng Z, Osborne DG, Li H, Dick CJ, Gomez TS, Koenecke M, Zhang JS, Dai H, Sifuentes-Dominguez LF, Geng LN, Kaufmann SH, Hein MY, Wallis M, McGaughran J, Gecz J, Sluis Bv, Billadeau DD, Burstein E. Mol Biol Cell. 2015 Jan 1;26(1):91-103.

Missense variant in CCDC22 causes X-linked recessive intellectual disability with - Missense variant in CCDC22 causes X-linked recessive intellectual disability with

Kolanczyk M, Krawitz P, Hecht J, Hupalowska A, Miaczynska M, Marschner K, Schlack C, Emmerich D, Kobus K, Kornak U, Robinson PN, Plecko B, Grangl G, Uhrig S, Mundlos S, Horn D. Eur J Hum Genet. 2015 May;23(5):633-8.

CCDC22: a novel candidate gene for syndromic X-linked intellectual disability. - CCDC22: a novel candidate gene for syndromic X-linked intellectual disability.

Voineagu I, Huang L, Winden K, Lazaro M, Haan E, Nelson J, McGaughran J, Nguyen LS, Friend K, Hackett A, Field M, Gecz J, Geschwind D. Mol Psychiatry. 2012 Jan;17(1):4-7.