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首页  >  重组蛋白  >  Human KRT13 Recombinant Protein
KRT13 (基因名), Keratin, type I cytoskeletal 13 (蛋白名), k1c13_human.
产品名称:

Human KRT13/ Keratin, type I cytoskeletal 13 Recombinant Protein
角蛋白,I型细胞骨架

货号:

R1875h

商标:
EIAab®
监管等级:
别名:

Cytokeratin-13, Keratin-13, CK-13, K13

序列号:
P13646
来源:
E.coli
种属:
Human
标签:
His
序列:
CMREQYEAMAERNRRDAEEW
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human KRT13 Protein
规格 & 价格: cart
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Human KRT13 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 17q21.2 by HGNC 17q21.2 by Entrez Gene 17q21.2 by Ensembl
KRT13 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Heterotetramer of two type I and two type II keratins. keratin-13 is generally associated with keratin-4.


功能:
N/A


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"Identification of two novel mutations in keratin 13 as the cause of white sponge naevus."

[2].
"Isolation, sequence and expression of the gene encoding human keratin 13."

[3].
"Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus."

[4].
"[Immunofluorescence examination of CK-13 expression in cell line KB differentiated by all-trans retinoic acid or As2 O3]."

[5].
"In situ adenocarcinoma and squamous carcinoma of uterine cervix. Pathological and immunohistochemical analysis with cytokeratin 13."

[6].
"New consensus nomenclature for mammalian keratins."

[7].
"Global, in vivo, and site-specific phosphorylation dynamics in signaling networks."

[8].
"[Cytokeratin18, 13 and their gene expression in post-operative maxillary cyst linings with metaplastic epithelium]."

[9].
"Complete sequencing and characterization of 21,243 full-length human cDNAs."

[10].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
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