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CDH3 Polyclonal Antibody

商品貨號(hào)： PLA019666

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說(shuō)明書

商品描述

基因名稱： CDH3 CDHP
蛋白名稱： Cadherin-3 (Placental cadherin) (P-cadherin)
Human_gene_id： 1001
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1001
Human_swiss_prot_no： P22223
Human_swiss_link： http://www.uniprot.org/uniprotkb/P22223/entry
Mouse_gene_id： 12560
Mouse_swiss_prot_no： P10287
Mouse_swiss_link： http://www.uniprot.org/uniprot/P10287
特異性： This antibody detects endogenous levels of CDH3.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)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(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： Cadherin-3 (Placental cadherin) (P-cadherin)
實(shí)測(cè)條帶： 120kD
信號(hào)通路： Cell adhesion molecules (CAMs);
功能： disease:Defects in CDH3 are the cause of ectodermal dysplasia with ectrodactyly and macular dystrophy (EEM) [MIM:225280]; also known as EEM syndrome, Albrectsen-Svendsen syndrome or Ohdo-Hirayama-Terawaki syndrome. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. EEM is an autosomal recessive condition characterized by features of ectodermal dysplasia such as sparse eyebrows and scalp hair, and selective tooth agenesis associated with macular dystrophy and ectrodactyly.,disease:Defects in CDH3 are the cause of hypotrichosis with juvenile macular dystrophy (HJMD) [MIM:601553]. HJMD is a rare autosomal recessive disorder characterized by early hair loss heralding severe degenerative changes of the retinal macula and culminating in blindness during the second to third decade of life.,function:Cadherins are calcium dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types.,online information:Retina International's Scientific Newsletter,similarity:Contains 5 cadherin domains.,subunit:Interacts with CDCP1.,tissue specificity:Expressed in some normal epithelial tissues and in some carcinoma cell lines.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane; Single-pass type I membrane protein.
組織表達(dá)： Expressed in some normal epithelial tissues and in some carcinoma cell lines.
tag： hot
科研貨號(hào)： PLA019666

CDH3 Polyclonal Antibody

Catalog No PLA019666

Product information

基因名稱： CDH3 CDHP
蛋白名稱： Cadherin-3 (Placental cadherin) (P-cadherin)
Human_gene_id： 1001
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=1001
Human_swiss_prot_no： P22223
Human_swiss_link： http://www.uniprot.org/uniprotkb/P22223/entry
Mouse_gene_id： 12560
Mouse_swiss_prot_no： P10287
Mouse_swiss_link： http://www.uniprot.org/uniprot/P10287
特異性： This antibody detects endogenous levels of CDH3.
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)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(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： Cadherin-3 (Placental cadherin) (P-cadherin)
實(shí)測(cè)條帶： 120kD
信號(hào)通路： Cell adhesion molecules (CAMs);
功能： disease:Defects in CDH3 are the cause of ectodermal dysplasia with ectrodactyly and macular dystrophy (EEM) [MIM:225280]; also known as EEM syndrome, Albrectsen-Svendsen syndrome or Ohdo-Hirayama-Terawaki syndrome. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. EEM is an autosomal recessive condition characterized by features of ectodermal dysplasia such as sparse eyebrows and scalp hair, and selective tooth agenesis associated with macular dystrophy and ectrodactyly.,disease:Defects in CDH3 are the cause of hypotrichosis with juvenile macular dystrophy (HJMD) [MIM:601553]. HJMD is a rare autosomal recessive disorder characterized by early hair loss heralding severe degenerative changes of the retinal macula and culminating in blindness during the second to third decade of life.,function:Cadherins are calcium dependent cell adhesion proteins. They preferentially interact with themselves in a homophilic manner in connecting cells; cadherins may thus contribute to the sorting of heterogeneous cell types.,online information:Retina International's Scientific Newsletter,similarity:Contains 5 cadherin domains.,subunit:Interacts with CDCP1.,tissue specificity:Expressed in some normal epithelial tissues and in some carcinoma cell lines.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane; Single-pass type I membrane protein.
組織表達(dá)： Expressed in some normal epithelial tissues and in some carcinoma cell lines.
tag： hot
科研貨號(hào)： PLA019666

Hunan UPT Biotechnology Co.,Ltd

Website：m.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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