PIPA5113794

NIPA2 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5113794-Each-of-1 In Stock ₹ 46,502.50

PIPA5113794 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

NIPA2

Classification

Polyclonal

Conjugate

Unconjugated

Gene

NIPA2

Gene Alias

2600017P10Rik; 3830408P04Rik; AB041581; Magnesium transporter NIPA2; MNCb-2146; Nipa2; non imprinted in Prader-Willi/Angelman syndrome 2; non imprinted in Prader-Willi/Angelman syndrome 2 homolog; non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human); non-imprinted in Prader-Willi/Angelman syndrome region protein 2; Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 homolog; RGD1306051

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

81614

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Immunohistochemistry, Western Blot

Concentration

0.5 mg/mL

Formulation

PBS with 2% sucrose and 0.09% sodium azide

Gene Accession No.

Q8N8Q9

Gene Symbols

NIPA2

Immunogen

Synthetic peptide directed towards the middle region of human NIPA2

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

IgG

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Description

  • Immunogen sequence: VYITICSVIG AFSVSCVKGL GIAIKELFAG KPVLRHPLAW ILLLSLIVCV For short term use, store at 2-8°C up to 1 week
  • For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles
  • Predicted homology: Cow: 93%; Dog: 100%; Guinea Pig: 79%; Horse: 100%; Human: 100%; Mouse: 86%; Pig: 100%; Rabbit: 100%; Rat: 86%; Zebrafish: 85% Nipa2 encodes a protein that acts as a selective Mg(2+) transporter
  • The Nipa2 gene encodes a possible magnesium transporter, and is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15
  • Alternate splicing of the Nipa2 gene results in multiple transcript variants
  • Pseudogenes of the Nipa2 gene are found on chromosomes 3, 7 and 21
  • Diseases associated with NIPA2 include Angelman Syndrome and Prader-Willi Syndrome.