KIF1BP Protein (His-GST)
Aperçu rapide pour KIF1BP Protein (His-GST) (ABIN7317164)
Antigène
Voir toutes KIF1BP (KIAA1279) ProtéinesType de proteíne
Origine
Source
Pureté
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Purification/Conjugué
- Cette KIF1BP protéine est marqué à la His-GST.
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Fonction
- Recombinant Human KIAA1279 Protein (His & GST Tag)
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Séquence
- Met 1-Thr621
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Attributs du produit
- A DNA sequence encoding the human KIAA1279 (Q96EK5) (Met1-Thr621) was expressed with the N-terminal polyhistidine-tagged GST tag at the N-terminus.
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Stérilité
- 0.2 μm filtered
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niveau d'endotoxine
- < 1.0 EU per μg of the protein as determined by the LAL method.
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Biological Activity Comment
- Not validated for activity
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Buffer
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Lyophilized from sterile 20 mM Tris, 500 mM NaCl, 10 % glycerol, pH 7.4
Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween 80 are added as protectants before lyophilization. -
Stock
- 4 °C,-20 °C,-80 °C
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Stockage commentaire
- Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
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Date de péremption
- 12 months
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- KIF1BP (KIAA1279) (KIAA1279)
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Autre désignation
- KIAA1279
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Sujet
- KBP,KIAA1279,TTC20,KIFBP (Kinesin Family Binding Protein, also known as KIAA1279 and KIF1BP) is a Protein Coding gene. This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratricopeptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating the transport of the mitochondria. Homozygous nonsense mutations in KIAA1279 at 1q22.1, encoding a protein with two tetratricopeptide repeats, underlie this syndromic form of Hirschsprung disease and generalized polymicrogyria, establishing the importance of KIAA1279 in both enteric and central nervous system development. KIAA1279 is widely expressed in the brain, testis, and other tissues. Diseases associated with KIFBP include Goldberg-Shprintzen Syndrome and Shprintzen-Goldberg Craniosynostosis Syndrome.
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Poids moléculaire
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Calculated MW: 99.6 kDa
Observed MW: 92-102 kDa
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ID gène
- 26128
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UniProt
- Q96EK5
Antigène
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