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RabbitAnti-LOXL1 Rabbit pAb  antibody (bs-18344R)
~~~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-18344R
英文名称 LOXL1 Rabbit pAb
中文名称 赖氨酰氧化酶样1抗体
别    名 LOL; LOXL; LOXL1_HUMAN; LOXL1; Lysyl oxidase-like protein 1 (LOL); 1.4.3.13; LOXL1_MOUSE; Lysyl oxidase 2; Lysyl oxidase-like protein 1; Lox2;   
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
克 隆 号
交叉反应 Mouse,  (predicted: Human, Rat, Dog, Pig, Cow, Horse, Rabbit, Sheep, )
产品应用 WB=1:500-2000 ELISA=1:5000-10000 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 53 kDa
检测分子量 53
细胞定位 分泌型蛋白 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human LOXL1: 401-500/574 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
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 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.

SWISS:
Q08397

Gene ID:
4016

Database links:

Entrez Gene: 4016 Human

Entrez Gene: 16949 Mouse

Entrez Gene: 315714 Rat

Omim: 153456 Human

SwissProt: Q08397 Human

SwissProt: P97873 Mouse



产品图片
Sample: Heart(Monse) Cell Lysate at 40 ug Primary: Anti-LOXL1(bs-18344R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 53 kD Observed band size: 53kD
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