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CCDC22 Rabbit pAb (bs-8124R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价
产品编号 bs-8124R
英文名称 CCDC22 Rabbit pAb
中文名称 卷曲螺旋结构域蛋白22抗体
别    名 CXorf37; JM1; RTSC2; DXImx40e; Ppp1r3f; Sfc22; RGD1560910; CCD22_HUMAN; CCDC22; CCD22_MOUSE; CCD22_RAT;   
研究领域 细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 Rat (predicted: Human,Mouse,Pig,Sheep,Cow,Dog,Horse)
产品应用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 71 kDa
细胞定位 细胞核 细胞浆 细胞外基质 分泌型蛋白 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from Human CCDC22: 525-627/627 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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].

Subunit:
Interacts with CPNE1 and CPNE4 (By similarity).

Tissue Specificity:
Widely expressed in adult tissues and in fetal liver and brain, with highest levels in prostate and lowest in skeletal muscle.

DISEASE:
Note=May be involved in X-linked syndromic mental retardation (PubMed:21826058). CCDC22 expression has been found to be down-regulated in a family with a phenotype consistent with X-linked syndromic mental retardation, and carrying variant Ala-17. In addition to intellectual disability, affected individuals have cardiac and skeletal abnormalities.

Similarity:
Belongs to the CCDC22 family.

SWISS:
O60826

Gene ID:
28952

Database links:

Entrez Gene: 28952 Human

Entrez Gene: 54638 Mouse

Entrez Gene: 317381 Rat

Omim: 300859 Human

SwissProt: O60826 Human

SwissProt: Q9JIG7 Mouse

SwissProt: P86182 Rat

Unigene: 247700 Human

Unigene: 26333 Human

Unigene: 288192 Mouse

Unigene: 38478 Rat



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