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Rabbit Anti-PGCP  antibody (bs-9917R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-9917R
英文名稱 Rabbit Anti-PGCP  antibody
中文名稱 血漿谷氨酸羧肽酶抗體
別    名 Plasma glutamate carboxypeptidase; CBPQ_HUMAN.  
研究領域 腫瘤  心血管  信號轉導  細胞外基質  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Rabbit)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:50-200,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 47kDa
細胞定位 分泌型蛋白 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human PGCP: 31-130/472 
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 PGCP is a 472 amino acid secreted protein that is primarily detected in blood plasma. PGCP is a carboxypeptidase that potentially is involved in the hydrolysis of circulating peptides. Due to its upregulation in hepatocellular carcinoma (HCC), it is suspected that PGCP may be a potential serological marker for HCC. PGCP is a member of the Peptidase M28 family of proteins, which also includes PSM (prostate-specific membrane antigen), metallopeptidases and aminopeptidases. The gene encoding PGCP maps to chromosome 8, which is made up of nearly 146 million bases and encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and are typically associated with a poor prognosis.In humans, PGCP is found principally in blood plasma. It is a Carboxypeptidase that may play an important role in the hydrolysis of circulating peptides.

Function:
Carboxypeptidase that may play an important role in the hydrolysis of circulating peptides. Catalyzes more efficiently the hydrolysis of dipeptides with unsubstituted terminals into amino acids. May play a role in thyroxin hormone liberation from its TG/thyroglobulin precursor.

Subunit:
Homodimer. The monomeric form is inactive while the homodimer is active.

Subcellular Location:
Secreted.

Tissue Specificity:
Mainly detected in blood plasma. Abundant in placenta and kidney. Present at low level in muscles, liver and skin fibroblasts. Not detected in brain or white blood cells (at protein level).

Post-translational modifications:
N-glycosylated. The secreted form is modified by hybrid or complex type oligosaccharide chains (By similarity).

Similarity:
Belongs to the peptidase M28 family.

SWISS:
Q9Y646

Gene ID:
10404

Database links:

Entrez Gene: 10404 Human

Entrez Gene: 54381 Mouse

Entrez Gene: 58952 Rat

SwissProt: Q9Y646 Human

SwissProt: Q9WVJ3 Mouse

SwissProt: Q6IRK9 Rat



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