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RabbitAnti-NIPAL4 Rabbit pAb  antibody (bs-19251R)
~~~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-19251R
英文名称 NIPAL4 Rabbit pAb
中文名称 镁转运蛋白NIPAL4抗体
别    名 ARCI6; ICHTHYIN; ICHYN; NIPA4; SLC57A6; 9530066K23Rik; NIPA4_HUMAN; NIPAL4; NIPA-like protein 4; Non-imprinted in Prader-Willi/Angelman syndrome region protein 4; ICHN; NIPA4_MOUSE; Non-imprinted in Prader-Willi/Angelman syndrome region protein 4 homolog;  
研究领域 肿瘤  细胞生物  免疫学  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 Human, Mouse,  (predicted: Rat, )
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 50 kDa
检测分子量 42
细胞定位 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NIPAL4: 331-430/466 <Extracellular>
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 likely encodes a membrane receptor. Mutations in this gene have been associated with autosomal recessive congenital ichthyosis. [provided by RefSeq, Feb 2010]

Function:
Acts as a Mg(2+) transporter. Can also transport other divalent cations such as Ba(2+), Mn(2+), Sr(2+) and Co(2+) but to a much less extent than Mg(2+) (By similarity). May be a receptor for ligands (trioxilins A3 and B3) from the hepoxilin pathway.

Subcellular Location:
Membrane.

Tissue Specificity:
Highly expressed in brain, lung, stomach, keratinocytes and leukocytes, and in all other tissues tested except liver, thyroid and fetal brain.

DISEASE:
Defects in NIPAL4 are the cause of ichthyosis congenital autosomal recessive ichthyin-related (ARCII) [MIM:612281]. ARCII is a disorder of keratinization with abnormal differentiation and desquamation of the epidermis. The phenotype usually presents as non-bullous congenital ichthyosiform erythroderma (NCIE) with fine whitish scaling on an erythrodermal background; larger brownish scales are present on the buttocks, neck and legs. Some of the families may show a more lamellar phenotype (lamellar ichthyosis).

Similarity:
Belongs to the NIPA family.

SWISS:
Q0D2K0

Gene ID:
348938

Database links:

Entrez Gene: 348938 Human

Entrez Gene: 214112 Mouse

Omim: 609383 Human

SwissProt: Q0D2K0 Human

SwissProt: Q8BZF2 Mouse

Unigene: 4285 Human



产品图片
Sample: A549(Human) Cell Lysate at 30 ug U251(Human) Cell Lysate at 30 ug Primary: Anti-NIPAL4 (bs-19251R) at 1/300 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 42 kD Observed band size: 42 kD
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