You are viewing an incomplete version of our website. Please click to reload the website as full version.

anti-Non Imprinted in Prader-Willi/Angelman Syndrome 2 Homolog (Human) (NIPA2) Antibodies

NIPA2 encodes a possible magnesium transporter. Additionally we are shipping and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
NIPA2 81614 Q8N8Q9
NIPA2 308667  
NIPA2 93790 Q9JJC8
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top anti-NIPA2 Antibodies at antibodies-online.com

Showing 6 out of 7 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Chicken Rabbit Un-conjugated WB WB Suggested Anti-NIPA2 Antibody Titration: 0.2-1 ug/mlELISA Titer: 1:312500Positive Control: 293T cell lysate 100 μL Log in to see 2 to 3 Days
$289.00
Details
Human Rabbit Un-conjugated WB 50 μg Log in to see 8 to 10 Days
$551.83
Details
Human Rabbit Un-conjugated ELISA, WB 50 μg Log in to see 2 to 3 Days
$433.13
Details
Human Rabbit Un-conjugated WB NIPA2 antibody used at 1 ug/ml to detect target protein. 50 μg Log in to see 3 to 4 Days
$473.93
Details
Human Rabbit Un-conjugated IHC, WB   0.1 mL Log in to see 8 to 11 Days
$439.69
Details
Human Rabbit Un-conjugated WB   20 μL Log in to see 6 to 9 Days
$191.63
Details

NIPA2 Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human


Rat (Rattus)


Mouse (Murine)


More Antibodies against NIPA2 Interaction Partners

Human Non Imprinted in Prader-Willi/Angelman Syndrome 2 Homolog (Human) (NIPA2) interaction partners

  1. This study primarily reveals that a selective magnesium transporter NIPA2 may play a role in the pathogenesis of CAE (show GJA8 Antibodies).

  2. mutations in NIPA2 gene were associated with childhood absence epilepsy (CAE (show GJA8 Antibodies)), which indicated that the haploinsufficiency of NIPA2 might be a candidate mechanism underlying the IGE/CAE (show GJA8 Antibodies) phenotypes caused by 15q11.2 microdeletions or rare mutations in NIPA2

  3. quantitated mRNA levels of NIPA2, NIPA2,l CYFIP1 (show CYFIP1 Antibodies), and GCP5 (show TUBGCP5 Antibodies) in Prader-Willi syndrome and correlated levels with psychological and behavior scales

Mouse (Murine) Non Imprinted in Prader-Willi/Angelman Syndrome 2 Homolog (Human) (NIPA2) interaction partners

  1. The isolation and characterization of Nipa2 in mouse distal convoluted tubule cells are reported.

NIPA2 Antigen Profile

Protein Summary

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.

Gene names and symbols associated with NIPA2

  • non imprinted in Prader-Willi/Angelman syndrome 2 (NIPA2) antibody
  • non imprinted in Prader-Willi/Angelman syndrome 2 (Nipa2) antibody
  • non imprinted in Prader-Willi/Angelman syndrome 2 (human) (nipa2) antibody
  • non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human) (Nipa2) antibody
  • 2600017P10Rik antibody
  • 3830408P04Rik antibody
  • AB041581 antibody
  • fb72g02 antibody
  • RGD1306051 antibody
  • wu:fb72g02 antibody
  • zgc:66088 antibody

Protein level used designations for NIPA2

magnesium transporter NIPA2 , non-imprinted in Prader-Willi/Angelman syndrome 2 , non-imprinted in Prader-Willi/Angelman syndrome region protein 2 , non-imprinted in Prader-Willi/Angelman syndrome region protein 2 homolog , non imprinted in Prader-Willi/Angelman syndrome 2 homolog

GENE ID SPECIES
418680 Gallus gallus
81614 Homo sapiens
479002 Canis lupus familiaris
507430 Bos taurus
308667 Rattus norvegicus
406399 Danio rerio
93790 Mus musculus
Selected quality suppliers for anti-NIPA2 (NIPA2) Antibodies
Did you look for something else?