先天性裂手/裂足畸形相关蛋白DSS1抗体

英文名称    DSS1    

中文名称    先天性裂手/裂足畸形相关蛋白DSS1抗体    

别    名    26S proteasome complex subunit DSS1; Deleted in split hand/split foot 1; Deleted in Split-Hand/Split-Foot 1 region; ECD; SEM1; SHFD1; DSS1_HUMAN; SHFM1; SHSF1; Split hand/foot deleted protein 1; Split hand/foot malformation (ectrodactyly) type 1; Split hand/foot malformation type 1 protein.    

说 明 书    0.2ml      

研究领域    细胞生物  发育生物学  细胞周期蛋白  泛素      

抗体来源    Rabbit    

克隆类型    Polyclonal    

交叉反应    Human, Pig, Cow, Rabbit,     

产品应用    ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 先天性裂手/裂足畸形相关蛋白DSS1抗体（石蜡切片需做抗原修复） 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.    

分 子 量    8.3kDa    

性    状    Lyophilized or Liquid    

浓    度    1mg/1ml    

免 疫 原    KLH conjugated synthetic peptide derived from human DSS1    

亚    型    IgG    

纯化方法    affinity purified by Protein A    

储 存 液    Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4    

保存条件    Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.    

先天性裂手/裂足畸形相关蛋白DSS1抗体产品介绍    background:

The product of this gene has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. It has been proposed to be a candidate gene for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. [provided by RefSeq, Jul 2008]

Function:
The gene for DSS1 has been localized within the split hand/split foot malformation locus SHFM1 at chromosome 7. DSS1 has been proposed to be a candidate for the autosomal dominant form of the heterogeneous limb developmental disorder split hand/split foot malformation type 1. In addition, it has been shown to directly interact with BRCA2. It also may play a role in the completion of the cell cycle. 

Subunit:
Part of the 26S proteasome. Interacts with the C-terminal of BRCA2.

Tissue Specificity:
Expressed in limb bud, craniofacial primordial and skin.

Similarity:
Belongs to the DSS1/SEM1 family.

Gene ID:
7979

Database links:

Entrez Gene: 7979 Human

Omim: 601285 Human

SwissProt: P60896 Human

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.    

先天性裂手/裂足畸形相关蛋白DSS1抗体

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