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RabbitAnti-KRT81 Rabbit pAb antibody (bs-20806R)
~~~促销,代码KXJ230206~~~
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价

产品编号 bs-20806R
英文名称 KRT81 Rabbit pAb
中文名称 细胞角蛋白81抗体
别    名 HB1; Hb-1; K81; KRTHB1; MLN137; MNLIX2; ghHkb1; hHAKB2-1; Krt2-19; KRT81_HUMAN; KRT81; Hair keratin K2.9; Keratin, hair, basic, 1; Keratin-81 (K81); Metastatic lymph node 137 gene protein (MLN 137); Type II hair keratin Hb1; Type-II keratin Kb21; ghHKb1 (ghHb1); KRT81_MOUSE; keratin 81; keratin 81, type II; hard keratin type II 1  
研究领域 细胞生物  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Mouse, 
产品应用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 55kDa
检测分子量 58
细胞定位 细胞浆 细胞外基质 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from mouse KRT81: 401/500/505 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 The protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle; this hair keratin, as well as KRTHB3 and KRTHB6, is found primarily in the hair cortex. Mutations in this gene and KRTHB6 have been observed in patients with a rare dominant hair disease, monilethrix. [provided by RefSeq, Jul 2008]

Function:
Abundantly expressed in the differentiating cortex of growing (anagen) hair. Expression is restricted to the keratinocytes of the hair cortex and is absent from inner root sheath and medulla. Expressed in malignant lymph node tissue in breast carcinoma tissue.

DISEASE:
Defects in KRT81 are a cause of monilethrix (MLTRX) [MIM:158000]. Monilethrix is an autosomal dominant hair disorder characterized clinically by alopecia and follicular papules. Affected hairs have uniform elliptical nodes of normal thickness and intermittent constrictions, internodes at which the hair easily breaks. Usually only the scalp is involved, but in severe forms, the secondary sexual hair, eyebrows, eyelashes, and nails may also be affected.

Similarity:
Belongs to the intermediate filament family.

SWISS:
Q9ERE2

Gene ID:
64818

Database links:

Entrez Gene: 3887 Human

Entrez Gene: 64818 Mouse

Omim: 602153 Human

SwissProt: Q14533 Human

SwissProt: Q9ERE2 Mouse

Unigene: 658118 Human

Unigene: 347934 Mouse



产品图片
Sample: Skin (Mouse) Lysate at 40 ug Primary: Anti-KRT81 (bs-20806R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 55 kD Observed band size: 58 kD
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