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BFSP1 rabbit pAb

商品貨號(hào)： PLA019849

適應(yīng) 性： 人,小鼠,大鼠

￥600元

規(guī)格：

40μL 100μL 200μL

在線(xiàn)咨詢(xún)

MSDS

說(shuō)明書(shū)

商品描述

基因名稱(chēng)： BFSP1
蛋白名稱(chēng)： BFSP1
Human_gene_id： 631
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=631
Human_swiss_prot_no： Q12934
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q12934/entry
Mouse_gene_id： 12075
Mouse_gene_link： https://www.uniprot.org/uniprot/12075
Mouse_swiss_prot_no： A2AMT1
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/A2AMT1
Rat_gene_id： 25394
Rat_gene_link： https://www.uniprot.org/uniprot/25394
Rat_swiss_prot_no： Q02435
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q02435
特異性： This antibody detects endogenous levels of BFSP1 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Polyclonal, Rabbit,IgG
稀釋?zhuān)? 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(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書(shū)： 1
Msds： MSDS_Antibody.pdf
分子量： 73kD
功能： disease:Defects in BFSP1 are the cause of autosomal recessive cortical juvenile-onset cataract [MIM:611391]. Cataract is the most frequent cause of visual impairment and blindness worldwide. While congenital cataracts are less frequent than age related cataracts, if not treated promptly they can result in irreversible neural blindness. The frequency of non-syndromic congenital cataract is estimated to be 1-6 cases per 10'000 children with one additional case being diagnosed during childhood. Developmental or juvenile onset cataract is distinguished from congenital cataract by initial clarity of the lens at birth and development of opacities progressively with maturation during childhood or adolescence. Approximately 25% of non-syndromic cataracts are inherited, and they are phenotypically and genetically heterogeneous, with autosomal dominant generally considered to be more common than autosomal recessive and X-linked inheritance.,similarity:Belongs to the intermediate filament family.,subcellular location:Membrane- and cytoskeleton-associated.,subunit:Associates with BFSP2.,tissue specificity:Lens.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane ; Peripheral membrane protein ; Cytoplasmic side . Cytoplasm . Cytoplasm, cytoskeleton . Cytoplasm, cell cortex .
組織表達(dá)： Expressed in the cortex and nucleus of the retina lens (at protein level).
科研貨號(hào)： PLA019849

BFSP1 rabbit pAb

Catalog No PLA019849

Product information

基因名稱(chēng)： BFSP1
蛋白名稱(chēng)： BFSP1
Human_gene_id： 631
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=631
Human_swiss_prot_no： Q12934
Human_swiss_link： https://www.uniprot.org/uniprotkb/Q12934/entry
Mouse_gene_id： 12075
Mouse_gene_link： https://www.uniprot.org/uniprot/12075
Mouse_swiss_prot_no： A2AMT1
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/A2AMT1
Rat_gene_id： 25394
Rat_gene_link： https://www.uniprot.org/uniprot/25394
Rat_swiss_prot_no： Q02435
Rat_swiss_link： https://www.uniprot.org/uniprotkb/Q02435
特異性： This antibody detects endogenous levels of BFSP1 at Human/Mouse/Rat
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來(lái)源： Polyclonal, Rabbit,IgG
稀釋?zhuān)? 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(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
說(shuō)明書(shū)： 1
Msds： MSDS_Antibody.pdf
分子量： 73kD
功能： disease:Defects in BFSP1 are the cause of autosomal recessive cortical juvenile-onset cataract [MIM:611391]. Cataract is the most frequent cause of visual impairment and blindness worldwide. While congenital cataracts are less frequent than age related cataracts, if not treated promptly they can result in irreversible neural blindness. The frequency of non-syndromic congenital cataract is estimated to be 1-6 cases per 10'000 children with one additional case being diagnosed during childhood. Developmental or juvenile onset cataract is distinguished from congenital cataract by initial clarity of the lens at birth and development of opacities progressively with maturation during childhood or adolescence. Approximately 25% of non-syndromic cataracts are inherited, and they are phenotypically and genetically heterogeneous, with autosomal dominant generally considered to be more common than autosomal recessive and X-linked inheritance.,similarity:Belongs to the intermediate filament family.,subcellular location:Membrane- and cytoskeleton-associated.,subunit:Associates with BFSP2.,tissue specificity:Lens.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3029
細(xì)胞定位： Cell membrane ; Peripheral membrane protein ; Cytoplasmic side . Cytoplasm . Cytoplasm, cytoskeleton . Cytoplasm, cell cortex .
組織表達(dá)： Expressed in the cortex and nucleus of the retina lens (at protein level).
科研貨號(hào)： PLA019849

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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