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WISP-3 Polyclonal Antibody

商品貨號： PLA019430

適應(yīng) 性： 人,大鼠,小鼠,

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： WISP3 CCN6 UNQ462/PRO790/PRO956
蛋白名稱： WNT1-inducible-signaling pathway protein 3 (WISP-3) (CCN family member 6)
Human_gene_id： 8838
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=8838
Human_swiss_prot_no： O95389
Human_swiss_link： http://www.uniprot.org/uniprotkb/O95389/entry
Mouse_gene_id： 327743
Mouse_swiss_prot_no： D3Z5L9
Mouse_swiss_link： http://www.uniprot.org/uniprot/D3Z5L9
特異性： The antibody detects endogenous WISP-3
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000, ELISA 1:10000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： WNT1-inducible-signaling pathway protein 3 (WISP-3) (CCN family member 6)
實測條帶： 55kD
功能： disease:Defects in WISP3 are the cause of progressive pseudorheumatoid arthropathy of childhood (PPAC) [MIM:208230]. PPAC is an autosomal recessive disorder characterized by stiffness and swelling of joints, motor weakness and joint contractures. Signs and symptoms of the disease develop typically between three and eight years of age. This progressive disease is a primary disorder of articular cartilage with continued cartilage loss and destructive bone changes with aging.,function:Appears to be required for normal postnatal skeletal growth and cartilage homeostasis.,similarity:Belongs to the CCN family.,similarity:Contains 1 CTCK (C-terminal cystine knot-like) domain.,similarity:Contains 1 IGFBP N-terminal domain.,similarity:Contains 1 TSP type-1 domain.,tissue specificity:Predominant expression in adult kidney and testis and fetal kidney. Weaker expression found in placenta, ovary, prostate and small intestine. Also expressed in skeletally-derived cells such as synoviocytes and articular cartilage chondrocytes.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Secreted . Mitochondrion . Associated with membranes. .
組織表達(dá)： Predominant expression in adult kidney and testis and fetal kidney. Weaker expression found in placenta, ovary, prostate and small intestine (PubMed:9843955, PubMed:10471507). Also expressed in skeletally-derived cells such as synoviocytes and articular cartilage chondrocytes (PubMed:10471507).
科研貨號： PLA019430

WISP-3 Polyclonal Antibody

Catalog No PLA019430

Product information

基因名稱： WISP3 CCN6 UNQ462/PRO790/PRO956
蛋白名稱： WNT1-inducible-signaling pathway protein 3 (WISP-3) (CCN family member 6)
Human_gene_id： 8838
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=8838
Human_swiss_prot_no： O95389
Human_swiss_link： http://www.uniprot.org/uniprotkb/O95389/entry
Mouse_gene_id： 327743
Mouse_swiss_prot_no： D3Z5L9
Mouse_swiss_link： http://www.uniprot.org/uniprot/D3Z5L9
特異性： The antibody detects endogenous WISP-3
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:500-2000, ELISA 1:10000-20000
純化工藝： The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： WNT1-inducible-signaling pathway protein 3 (WISP-3) (CCN family member 6)
實測條帶： 55kD
功能： disease:Defects in WISP3 are the cause of progressive pseudorheumatoid arthropathy of childhood (PPAC) [MIM:208230]. PPAC is an autosomal recessive disorder characterized by stiffness and swelling of joints, motor weakness and joint contractures. Signs and symptoms of the disease develop typically between three and eight years of age. This progressive disease is a primary disorder of articular cartilage with continued cartilage loss and destructive bone changes with aging.,function:Appears to be required for normal postnatal skeletal growth and cartilage homeostasis.,similarity:Belongs to the CCN family.,similarity:Contains 1 CTCK (C-terminal cystine knot-like) domain.,similarity:Contains 1 IGFBP N-terminal domain.,similarity:Contains 1 TSP type-1 domain.,tissue specificity:Predominant expression in adult kidney and testis and fetal kidney. Weaker expression found in placenta, ovary, prostate and small intestine. Also expressed in skeletally-derived cells such as synoviocytes and articular cartilage chondrocytes.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Secreted . Mitochondrion . Associated with membranes. .
組織表達(dá)： Predominant expression in adult kidney and testis and fetal kidney. Weaker expression found in placenta, ovary, prostate and small intestine (PubMed:9843955, PubMed:10471507). Also expressed in skeletally-derived cells such as synoviocytes and articular cartilage chondrocytes (PubMed:10471507).
科研貨號： PLA019430

Hunan UPT Biotechnology Co.,Ltd

Website：www.tjdqdt.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.

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