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GOLPH3 Rabbit pAb (bs-13488R)  
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產品編號 bs-13488R
英文名稱 GOLPH3 Rabbit pAb
中文名稱 高爾基體磷蛋白3抗體
別    名 Coat protein GPP34; FLJ90675; Golgi peripheral membrane protein 1, 34 kDa; Golgi phosphoprotein 3(coat protein); Golgi phosphoprotein 3; GOLP3_HUMAN; Golph3; GPP34; MIDAS; Mitochondrial DNA absence factor.  
研究領域 腫瘤  細胞生物  信號轉導  細胞類型標志物  細胞膜蛋白  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應 Human (predicted: Mouse,Rat,Cow,Chicken,Dog,Horse)
產品應用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 34 kDa
檢測分子量
細胞定位 細胞漿 細胞膜 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human GOLPH3: 51-150/298 
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 Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. GOLPH3L (golgi phosphoprotein 3-like), also known as GPP34R, is a 285 amino acid cytoplasmic protein that localizes to the Golgi apparatus. Belonging to the GOLPH3/VPS74 family, GOLPH3L may have a regulatory role in Golgi trafficking. GOLPH3L is encoded by a gene located on human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

Function:
Involved in modulation of mTOR signaling. Involved in the regulation of mitochondrial lipids, leading to increase of mitochondrial mass. Potential oncogene.

Subunit:
Homodimer. Interacts with VPS35.

Subcellular Location:
Cell membrane. Endosome. Cytoplasm. Golgi apparatus > Golgi stack membrane. Mitochondrion intermembrane space.

Tissue Specificity:
Detected in muscle fibers of patients with mitochondrial diseases; not detected in normal muscle fibers.

Post-translational modifications:
Phosphorylated.

Similarity:
Belongs to the GOLPH3/VPS74 family.

SWISS:
Q9H4A6

Gene ID:
64083

Database links:

Entrez Gene: 64083 Human

Entrez Gene: 531359 Cow

Entrez Gene: 66629 Mouse

Entrez Gene: 78961 Rat

Omim: 612207 Human

SwissProt: Q9H4A6 Human

SwissProt: Q9CRA5 Mouse

SwissProt: Q9ERE4 Rat

Unigene: 408909 Human

Unigene: 250936 Mouse

Unigene: 64519 Rat



產品圖片
Sample: Hela(Human) Cell Lysate at 30 ug Primary: Anti- GOLPH3 (bs-13488R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 34 kD Observed band size: 33 kD
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