NIPA1 antibody (C-Term)
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- Target See all NIPA1 Antibodies
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
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Binding Specificity
- C-Term
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Reactivity
- Human, Mouse, Dog, Guinea Pig, Horse, Rat, Cow
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This NIPA1 antibody is un-conjugated
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Application
- Western Blotting (WB)
- 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
- Top Product
- Discover our top product NIPA1 Primary Antibody
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- Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
- Comment
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Antigen size: 254 AA
- Restrictions
- For Research Use only
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- 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.
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- Target
- NIPA1 (Non Imprinted In Prader Willi/Angelman Syndrome Region Protein 1 (NIPA1))
- Alternative Name
- NIPA1 (NIPA1 Products)
- Synonyms
- FSP3 antibody, SPG6 antibody, 1110027G09Rik antibody, A830014A18Rik antibody, Spg6 antibody, non imprinted in Prader-Willi/Angelman syndrome 1 antibody, non imprinted in Prader-Willi/Angelman syndrome 1 homolog (human) antibody, NIPA1 antibody, Nipa1 antibody
- Background
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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
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