Major Facilitator Superfamily Domain Containing 8 (MFSD8) Peptide
MFSD8
Reactivité: Mammifères
Hôte: Synthetic
BP, WB, IHC
N° du produit ABIN938277
Aperçu rapide pour Major Facilitator Superfamily Domain Containing 8 (MFSD8) Peptide (ABIN938277)
Antigène
MFSD8
(Major Facilitator Superfamily Domain Containing 8 (MFSD8))
Origine
Mammifères
Source
Synthetic
Application
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
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Type de proteíne
- Synthetic
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Séquence
- FFILLPWGNQ FPKIQWEDLH NNSIPNTTFG EIIIGLWKSP MEDDNERPTG
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Attributs du produit
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A synthetic peptide for use as a blocking control in assays to test for specificity of MFSD8 antibody,
Alternative Names: MFSD8 control peptide, MFSD8 antibody Blocking Peptide, Anti-MFSD8 Blocking Peptide, major facilitator superfamily domain containing 8 Blocking Peptide, CLN7 Blocking Peptide, MGC33302 Blocking Peptide, MFSD8, MFSD-8, MFSD 8, MFSD-8 Blocking Peptide, MFSD 8 Blocking Peptide -
Purification
- The antibody is affinity-purified from rabbit antiserum by affinity chromatography using epitope-specific phosphopeptide. The antibody against non-phosphopeptide is removed by chromatogramphy using non-phosphopeptide corresponding to the phosphorylation site.
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Indications d'application
- Optimal conditions should be determined by the investigator
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
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Buffer
- PBS
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Conseil sur la manipulation
- Avoid repeated freeze/thaw cycles.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20 °C long term.
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- MFSD8 (Major Facilitator Superfamily Domain Containing 8 (MFSD8))
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Sujet
- This gene encodes a ubiquitous integral membrane protein that contains a transporter domain and a major facilitator superfamily (MFS) domain. Other members of the major facilitator superfamily transport small solutes through chemiosmotic ion gradients. The substrate transported by this protein is unknown. The protein likely localizes to lysosomal membranes. Mutations in this gene are correlated with a variant form of late infantile-onset neuronal ceroid lipofuscinoses (vLINCL).
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Poids moléculaire
- 57 kDa
Antigène
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