NIPA1 antibody (C-Term)

Catalog No. ABIN2789860

This Rabbit Polyclonal antibody specifically detects NIPA1 in WB. It exhibits reactivity toward Human, Mouse, Dog, Guinea Pig, Horse, Rat and Cow.

Quick Overview for NIPA1 antibody (C-Term) (ABIN2789860)

Target: NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))

Reactivity: Human, Mouse, Dog, Guinea Pig, Horse, Rat, Cow

Host: Rabbit

Clonality: Polyclonal

Conjugate: This NIPA1 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-NIPA1 Antibody

Binding Specificity: C-Term

Sequence: FREWSNVGLV DFLGMACGFT TVSVGIVLIQ VFKEFNFNLG EMNKSNMKTD

Predicted Reactivity: Cow: 93%, Dog: 100%, Guinea Pig: 100%, Horse: 100%, Human: 100%, Mouse: 100%, Rat: 100%

Characteristics: This is a rabbit polyclonal antibody against NIPA1. It was validated on Western Blot.

Purification: Affinity Purified

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator.

Comment:

Antigen size: 254 AA

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freeze-thaw cycles.

Storage: -20 °C

Storage Comment: 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.

Target Details for NIPA1

Target: NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))

Alternative Name: NIPA1

Background: This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6.
Alias Symbols: FSP3, MGC102724, MGC35570, SPG6
Protein Size: 254

Molecular Weight: 27 kDa

Gene ID: 123606

NCBI Accession: NM_001142275, NP_001135747