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Rabbit Anti-NIPA-2 antibody
Rabbit Anti-NIPA-2 antibody
Magnesium transporter NIPA2; MGC5466; NIPA 2; NIPA2_HUMAN; NIPA2;Non imprinted in Prader Willi/Angelman syndrome 2; Non imprinted in Prader Willi/Angelman syndrome region protein 2.
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  • NO.:SL7465R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,(predicted: Mouse,Rat,Chicken,Dog,Cow,Rabbit,)
    Applications:WB ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name NIPA-2
Chinese Name 镁TransporterNIPA2抗体
Alias Magnesium transporter NIPA2; MGC5466; NIPA 2; NIPA2_HUMAN; NIPA2; Non imprinted in Prader Willi/Angelman syndrome 2; Non imprinted in Prader Willi/Angelman syndrome region protein 2.  
Research Area Tumour  Cell biology  immunology  Signal transduction  The new supersedes the old  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human,  (predicted: Mouse, Rat, Chicken, Dog, Cow, Rabbit, )
Applications 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 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 36kDa
Cellular localization The cell membrane 
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human NIPA-2: 251-360/360 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010]

Function:
This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21.

Subcellular Location:
Membrane; Multi-pass membrane protein.

Tissue Specificity:
Widely expressed.

Similarity:
Belongs to the NIPA family.

SWISS:
Q8N8Q9

Gene ID:
81614

Database links:

Entrez Gene: 81614 Human

Entrez Gene: 507430 Cow

Entrez Gene: 479002 Dog

Entrez Gene: 93790 Mouse

Omim: 608146 Human

SwissProt: Q3SWXO Cow

SwissProt: Q8N8Q9 Human

SwissProt: Q9JJC8 Mouse

Unigene: 591003 Human



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