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Rabbit Anti-ZDHHC15  antibody (bs-18478R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-18478R
英文名稱 Rabbit Anti-ZDHHC15  antibody
中文名稱 ZDHHC15蛋白抗體
別    名 DHHC-15; Palmitoyltransferase ZDHHC15; UNQ1969/PRO4501; ZDH15_HUMAN; Zdhhc15; Zinc finger DHHC domain-containing protein 15.  
研究領域 心血管  細胞生物  免疫學  神經生物學  轉錄調節因子  鋅指蛋白  表觀遺傳學  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Dog,Horse)
產品應用 IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=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.
理論分子量 39kDa
細胞定位 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ZDHHC15: 201-300/337 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產品介紹 The protein encoded by this gene belongs to the DHHC palmitoyltransferase family. Mutations in this gene are associated with mental retardatio X-linked type 91 (MRX91). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

Function:
Palmitoyltransferase specific for GAP43 and DLG4/PSD95.

Subcellular Location:
Membrane.

Post-translational modifications:
Autopalmitoylated.

DISEASE:
Defects in ZDHHC15 are the cause of mental retardation X-linked type 91 (MRX91) [MIM:300577]. Mental retardation is characterized by significantly sub-average general intellectual functioning associated with impairments in adaptative behavior and manifested during the developmental period. Non-syndromic mental retardation patients do not manifest other clinical signs.

Similarity:
Belongs to the DHHC palmitoyltransferase family.
Contains 1 DHHC-type zinc finger.

SWISS:
Q96MV8

Gene ID:
158866

Database links:

Entrez Gene: 158866 Human

Omim: 300576 Human

SwissProt: Q96MV8 Human

Unigene: 253211 Human



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