CCDC22 Mouse Monoclonal Antibody [Kloon ID: LBI1B4]

This gene encodes a protein containing a coiled-coil domain. The encoded protein functions in the regulation of NF-kB (nuclear factor kappa-light-chain-enhancer of activated B cells) by interacting with COMMD (copper metabolism Murr1 domain-containing) proteins. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2013]

Carrier-free (BSA/glycerol-free) CCDC22 mouse monoclonal antibody, clone LBI1B4

CXorf37; JM1; RTSC2

Homo sapiens coiled-coil domain containing 22 (CCDC22), mRNA.

28952

O60826

Unconjugated

WB 1:2000

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

CCDC22

https://www.ncbi.nlm.nih.gov/gene/?term=28952

https://www.uniprot.org/uniprot/O60826