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CIR1A rabbit pAb

商品貨號： PLA020784

適應(yīng) 性： 人,小鼠

￥600元

規(guī)格：

40μL 100μL 200μL

在線咨詢

MSDS

說明書

商品描述

基因名稱： CIRH1A KIAA1988
蛋白名稱： CIR1A
Human_gene_id： 84916
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=84916
Human_swiss_prot_no： Q969X6
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q969X6/entry
Mouse_gene_id： 21771
Mouse_gene_link： https://www.uniprot.org/uniprot/21771
Mouse_swiss_prot_no： Q8R2N2
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q8R2N2
特異性： This antibody detects endogenous levels of CIR1A at Human/Mouse
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
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
分子量： 75kD
功能： disease:Defects in CIRH1A are the cause of North American Indian childhood cirrhosis (NAIC) [MIM:604901]. NAIC is a severe autosomal recessive intrahepatic cholestasis, originally described in Ojibway-Cree children from northwestern Quebec. NAIC typically presents with transient neonatal jaundice, in a child who is otherwise healthy, and progresses to biliary cirrhosis and portal hypertension. Biochemical and histopathological features suggest involvement of the bile ducts rather than of the bile canaliculi. They include elevated gamma glutamyltransferase and alkaline phosphatase levels, and, typically, marked fibrosis around bile ducts. Clinically, NAIC is distinct from other nonsyndromic familial cholestases because of its marked cholangiopathic features and severe degree of fibrosis on liver histology.,similarity:Contains 11 WD repeats.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Nucleus, nucleolus . Chromosome . Found predominantly at the fibrillar center. .
科研貨號： PLA020784

CIR1A rabbit pAb

Catalog No PLA020784

Product information

基因名稱： CIRH1A KIAA1988
蛋白名稱： CIR1A
Human_gene_id： 84916
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=84916
Human_swiss_prot_no： Q969X6
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q969X6/entry
Mouse_gene_id： 21771
Mouse_gene_link： https://www.uniprot.org/uniprot/21771
Mouse_swiss_prot_no： Q8R2N2
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q8R2N2
特異性： This antibody detects endogenous levels of CIR1A at Human/Mouse
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
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
分子量： 75kD
功能： disease:Defects in CIRH1A are the cause of North American Indian childhood cirrhosis (NAIC) [MIM:604901]. NAIC is a severe autosomal recessive intrahepatic cholestasis, originally described in Ojibway-Cree children from northwestern Quebec. NAIC typically presents with transient neonatal jaundice, in a child who is otherwise healthy, and progresses to biliary cirrhosis and portal hypertension. Biochemical and histopathological features suggest involvement of the bile ducts rather than of the bile canaliculi. They include elevated gamma glutamyltransferase and alkaline phosphatase levels, and, typically, marked fibrosis around bile ducts. Clinically, NAIC is distinct from other nonsyndromic familial cholestases because of its marked cholangiopathic features and severe degree of fibrosis on liver histology.,similarity:Contains 11 WD repeats.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Nucleus, nucleolus . Chromosome . Found predominantly at the fibrillar center. .
科研貨號： PLA020784

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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