Rabbit Anti-NIPA-2 antibody

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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.

Cat:

SL7465R

Species Reactivity：

Human,(predicted: Mouse,Rat,Chicken,Dog,Cow,Rabbit,)

Immunogen：

KLH conjugated synthetic peptide derived from human NIPA-2:251-360/360

Format：

Liquid

Storage instructions：

Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.

Concentration：

1mg/ml

Clonality：

Polyclonal

Isotype：

IgG

Applications：

WB=1:500-2000ELISA=1:5000-10000IHC-P=1:100-500IHC-F=1:100-500ICC=1:100-500IF=1:100-500（Paraffin sections need to do antigen repair）not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.

Host：

Rabbit

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Unit:

Price: $228.00

Product PDFs

Datasheet: Down Datasheet

Other Information
Citations
Protein Attributes
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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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