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RabbitAnti-COX4NB Rabbit pAb  antibody (bs-8310R)
~~~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-8310R
英文名称 COX4NB Rabbit pAb
中文名称 COX4NB蛋白抗体
别    名 C16orf2; C16orf4; COX4NB; FAM158B; NOC4; DD6A4-2(5); EMC8_HUMAN; EMC8; Neighbor of COX4; Protein FAM158B; COX4AL; EMC8_MOUSE; EMC8_RAT;   
研究领域 细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 (predicted: Human, Mouse, Rat, Dog, Pig, Cow, Rabbit, )
产品应用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=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 24 kDa
细胞定位 细胞浆 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human COX4NB: 121-210/210 
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 COX4NB is a 210 amino acid protein encoded by the human gene COX4NB. COX4NB belongs to the UPF0172 (NOC4) family and is found on chromosome 16, adjacent to the gene that encodes COX4. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16 through the CREBBP gene which encodes a critical CREB binding protein. Crohn’s disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other auto-immune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

Subunit:
Component of the ER membrane protein complex (EMC).

Subcellular Location:
Cytoplasm.

Tissue Specificity:
Expressed in liver, pancreas, heart, lung, kidney, brain, skeletal muscle, and placenta. Expression levels are highest in pancreas and moderate in heart, skeletal muscle, and placenta.

Similarity:
Belongs to the EMC8/EMC9 family.

SWISS:
O43402

Gene ID:
10328

Database links:

Entrez Gene: 10328 Human

Entrez Gene: 18117 Mouse

Entrez Gene: 361425 Rat

Omim: 604886 Human

SwissProt: O43402 Human

SwissProt: O70378 Mouse

SwissProt: Q5FVL2 Rat

Unigene: 173162 Human

Unigene: 2136 Mouse

Unigene: 6292 Rat



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