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PRSS1 Rabbit pAb (bs-8744R)  
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50ul/1180.00元
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產(chǎn)品編號(hào) bs-8744R
英文名稱 PRSS1 Rabbit pAb
中文名稱 絲氨酸蛋白酶1抗體
別    名 alpha trypsin chain 1; alpha-trypsin chain 1; alpha-trypsin chain 2; beta-trypsin; beta trypsin; Cationic trypsinogen; Serine protease 1; Serine protease-1; TRP1; TRY1; TRY1_HUMAN; TRYP1; Trypsin I; Trypsin-I; Trypsin 1; Trypsin-1.  
研究領(lǐng)域 細(xì)胞生物  泛素  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號(hào)
交叉反應(yīng) Human (predicted: Dog)
產(chǎn)品應(yīng)用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 27 kDa
檢測(cè)分子量
細(xì)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 PRSS1: 51-150/247 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 This gene encodes a trypsinogen, which is a member of the trypsin family of serine proteases. This enzyme is secreted by the pancreas and cleaved to its active form in the small intestine. It is active on peptide linkages involving the carboxyl group of lysine or arginine. Mutations in this gene are associated with hereditary pancreatitis. This gene and several other trypsinogen genes are localized to the T cell receptor beta locus on chromosome 7. [provided by RefSeq, Jul 2008]

Function:
Has activity against the synthetic substrates Boc-Phe-Ser-Arg-Mec, Boc-Leu-Thr-Arg-Mec, Boc-Gln-Ala-Arg-Mec and Boc-Val-Pro-Arg-Mec. The single-chain form is more active than the two-chain form against all of these substrates.

Subcellular Location:
Secreted > extracellular space.

Post-translational modifications:
Occurs in a single-chain form and a two-chain form, produced by proteolytic cleavage after Arg-122.

DISEASE:
Defects in PRSS1 are a cause of hereditary pancreatitis (HPC) [MIM:167800]; also known as chronic pancreatitis (CP). HPC is an autosomal dominant disease characterized by the presence of calculi in pancreatic ducts. It causes severe abdominal pain attacks.

Similarity:
Belongs to the peptidase S1 family.
Contains 1 peptidase S1 domain.

SWISS:
P07477

Gene ID:
5644

Database links:

Entrez Gene: 5644 Human

Entrez Gene: 114228 Mouse

Entrez Gene: 24691 Rat

Omim: 276000 Human

SwissProt: P00760 Cow

SwissProt: P07477 Human

SwissProt: P00762 Rat

Unigene: 449281 Human

Unigene: 449428 Mouse

Unigene: 34435 Rat



產(chǎn)品圖片
Paraformaldehyde-fixed, paraffin embedded (Human liver carcinoma); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (PRSS1) Polyclonal Antibody, Unconjugated (bs-8744R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
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