Protein name:
Calcium-binding protein 4 (CaBP4) ;
Alternative:
Organism:
Human (Homo sapiens).
General Annotation
Sub Unit:
Interacts with CACNA1F and CACNA1D (via IQ domain) in a calcium independent manner (By similarity). Interacts (via N-terminus) with UNC119.
Function:
Involved in normal synaptic function through regulation of Ca(2+) influx and neurotransmitter release in photoreceptor synaptic terminals and in auditory transmission. Modulator of CACNA1D and CACNA1F, suppressing the calcium-dependent inactivation and shifting the activation range to more hyperpolarized voltages.
Subcellular Location:
Cytoplasm
Found in rod spherules and cone pedicles of the presynapses from both types of photoreceptors.
Protein Attributes:
50:
MTTEQARGQQ | GPNLAIGRQK | PPAGVVTPKS | DAEEPPLTRK | RSKKERGLRG |
100:
SRKRTGSSGE | QTGPEAPGSS | NNPPSTGEGP | AGAPPASPGP | ASSRQSHRHR |
150:
PDSLHDAAQR | TYGPLLNRVF | GKDRELGPEE | LDELQAAFEE | FDTDRDGYIS |
200:
HRELGDCMRT | LGYMPTEMEL | LEVSQHIKMR | MGGRVDFEEF | VELIGPKLRE |
250:
ETAHMLGVRE | LRIAFREFDR | DRDGRITVAE | LREAVPALLG | EPLAGPELDE |
275:
MLREVDLNGD | GTVDFDEFVM | MLSRH
Vaild Sequence:
Related Databases
Uniprot:
ELISA Kit
CLIA Kit
Polyclonal Antibody
Monoclonal Antibody
Protein
FOR
Human
Mouse
Bovine
ELISA Kit for Human CaBP4
ELISA Kit for Human CaBP4
ELISA Kit for Human CaBP4
Polyclonal Antibody for Human CaBP4
Polyclonal Antibody for Human CaBP4
Polyclonal Antibody for Human CaBP4
Monoclonal Antibody for Human CaBP4
Monoclonal Antibody for Human CaBP4
Monoclonal Antibody for Human CaBP4
R&D Technical Data
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Precision
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Recovery
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Linearity
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References
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
Cited for : NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2)
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[15/1/25 17:38] Upload to ab completed in less than a minute: 1 file transferred (13.4 Kb/s)
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Cited for : SUBCELLULAR LOCATION
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"Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness."
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Cited for : VARIANT CSNB2B CYS-124