CCDC22 抗体
(Coiled-Coil Domain Containing 22 (CCDC22))
This gene encodes a protein containing a coiled-coil domain. The mouse orthologous protein has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. Localization of the orthologous rat protein suggests that it may play a role in neuronal injury response. This human gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability. [provided by RefSeq, Aug 2011].
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30 results :
CCDC22
适用: 人
WB, IHC (p)
宿主: 兔
Polyclonal
RB33346
unconjugated
CCDC22
适用: 小鼠, 大鼠
WB, ELISA, IF (cc), IF (p), IHC (p), IHC (fro)
宿主: 兔
Polyclonal
unconjugated
CCDC22
适用: 小鼠, 大鼠
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 488
CCDC22
适用: 小鼠, 大鼠
WB, ELISA, IHC (p), IHC (fro)
宿主: 兔
Polyclonal
Biotin
CCDC22
适用: 小鼠, 大鼠
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 750
CCDC22
适用: 小鼠, 大鼠
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 680
CCDC22
适用: 小鼠, 大鼠
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 594
CCDC22
适用: 小鼠, 大鼠
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 647
CCDC22
适用: 小鼠, 大鼠
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 555
CCDC22
适用: 小鼠, 大鼠
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 350
Latest Publications for our CCDC22 抗体
: "Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome." in: European journal of human genetics : EJHG, Vol. 23, Issue 5, pp. 720, (2015) (PubMed).Aliases for CCDC22 抗体
coiled-coil domain containing 22 (CCDC22) 抗体coiled-coil domain containing 22 (Ccdc22) 抗体
coiled-coil domain containing 22 (ccdc22) 抗体
AI481216 抗体
CXorf37 抗体
DXImx40e 抗体
Ppp1r3f 抗体
RGD1560910 抗体
Sfc22 抗体
zgc:114058 抗体
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