FITC标记的赖氨酰氧化酶样1抗体-抗体-抗体-生物在线
上海沪震实业有限公司
FITC标记的赖氨酰氧化酶样1抗体

FITC标记的赖氨酰氧化酶样1抗体

商家询价

产品名称: FITC标记的赖氨酰氧化酶样1抗体

英文名称: Anti-LOXL1/FITC

产品编号: HZ-18344R-FITC

产品价格: null

产品产地: 中国/上海

品牌商标: HZbscience

更新时间: 2023-08-17T10:24:20

使用范围: ICC=1:50-200 IF=1:50-200

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 Rabbit Anti-LOXL1/FITC Conjugated antibody 

FITC标记的赖氨酰氧化酶样1抗体

 

英文名称 Anti-LOXL1/FITC
中文名称 FITC标记的赖氨酰氧化酶样1抗体
别    名 Lysyl oxidase like 1; LOL; LOXL1_HUMAN; LOXL; Lysyl oxidase homolog 1; Lysyl oxidase like 1; Lysyl oxidase like protein 1.  
规格价格 100ul/2980元 购买        大包装/询价
说 明 书 100ul  
研究领域 肿瘤  细胞生物  免疫学  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, 
产品应用 ICC=1:50-200 IF=1:50-200  
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 53kDa
性    状 Lyophilized or Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human LOXL1
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
产品介绍 background:
This gene encodes a member of the lysyl oxidase gene family. The prototypic member of the family is essential to the biogenesis of connective tissue, encoding an extracellular copper-dependent amine oxidase that catalyses the first step in the formation of crosslinks in collagens and elastin. A highly conserved amino acid sequence at the C-terminus end appears to be sufficient for amine oxidase activity, suggesting that each family member may retain this function. The N-terminus is poorly conserved and may impart additional roles in developmental regulation, senescence, tumor suppression, cell growth control, and chemotaxis to each member of the family. [provided by RefSeq, Jul 2008]

Function:
Involved in hearing. Required for normal function of hair cells in the inner ear.

Subcellular Location:
Secreted, extracellular space.

DISEASE:
Deafness, autosomal recessive, 77 (DFNB77) [MIM:613079]: A form of non-syndromic deafness characterized by preserved low-frequency hearing, and a trend toward mild to moderate mid-frequency and high-frequency hearing loss during childhood and adolescence. Hearing loss progresses to become moderate to severe at mid and high frequencies during adulthood.

Similarity:
Contains 14 PLAT domains. 

Database links:

Entrez Gene: 4016 Human

Entrez Gene: 16949 Mouse

Entrez Gene: 315714 Rat

Omim: 153456 Human

SwissProt: Q08397 Human

SwissProt: P97873 Mouse



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications
   

该基因编码赖氨酰氧化酶基因家族的一个成员。该家族的原型成员对于结缔组织的生物发生是必不可少的,编码细胞外铜依赖的胺氧化酶,该酶催化胶原和弹性蛋白形成交联的第一步。在C末端的高度保守的氨基酸序列似乎对胺氧化酶活性足够,表明每个家族成员可能保留这个功能。N端保守性差,可能给每个家族成员在发育调节、衰老、肿瘤抑制、细胞生长控制和趋化性方面赋予额外的作用。[ RefSeq,JUL 2008 ]