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KBP rabbit pAb

CAT: 0855-ES15358-01Size: 50 µLDry Ice: NoHazardous: No
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CAT#:0855-ES15358-01Size:50 µL
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Background
This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome. [provided by RefSeq, Mar 2010]
Description
This gene encodes a kinesin family member 1 binding protein that is characterized by two tetratrico peptide repeats. The encoded protein localizes to the mitochondria and may be involved in regulating transport of the mitochondria. Mutations in this gene are associated with Goldberg-Shprintzen megacolon syndrome. [provided by RefSeq, Mar 2010],
UniProt
Q96EK5
Swiss Prot
Q96EK5
Reactivity
Human; Mouse; Rat
Immunogen
Synthesized peptide derived from human KBP AA range: 542-592
Target
KBP
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC
Concentration
1 mg/ml
Dilution
WB 1:500-2000; IHC-p 1:50-300
Buffer
-20°C/1 year
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Cytoplasm, cytoskeleton .
Gene ID (Human)
26128

UniProtKB · Q96EK5

KIF-binding protein

KBP_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q96EK5
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
KIFBP
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A8K5M8, Q9BR89, Q9ULE1, Q9Y428
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Cellular component

CytoplasmCytoskeleton

Molecular function

Developmental protein

Biological process

DifferentiationNeurogenesis

Disease

Hirschsprung disease

PTM

Phosphoprotein

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