KIF1BP Protein (His-GST)
Quick Overview for KIF1BP Protein (His-GST) (ABIN7317164)
Target
See all KIF1BP (KIAA1279) ProteinsProtein Type
Origin
Source
Purity
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Purification tag / Conjugate
- This KIF1BP protein is labelled with His-GST.
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Purpose
- Recombinant Human KIAA1279 Protein (His & GST Tag)
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Sequence
- Met 1-Thr621
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Characteristics
- 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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Sterility
- 0.2 μm filtered
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Endotoxin Level
- < 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. -
Storage
- 4 °C,-20 °C,-80 °C
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Storage Comment
- 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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Expiry Date
- 12 months
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- KIF1BP (KIAA1279) (KIAA1279)
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Alternative Name
- KIAA1279
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Background
- 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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Molecular Weight
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Calculated MW: 99.6 kDa
Observed MW: 92-102 kDa
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Gene ID
- 26128
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UniProt
- Q96EK5
Target
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