Home > Product > Antibody > Rabbit Anti-KBP antibody
Hypothetical protein LOC26128; KBP; KBP_HUMAN; KIAA1279; KIF1-binding protein; TTC20; Uncharacterized protein KIAA1279.
Cat:
SL9716R
Species Reactivity:
Human,(predicted: Mouse,Rat,Horse,)
Immunogen:
KLH conjugated synthetic peptide derived from human KBP:151-250/621
Format:
Liquid
Storage instructions:
Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Concentration:
1mg/ml
Clonality:
Polyclonal
Isotype:
IgG
Applications:
WB=1:500-2000ELISA=1:5000-10000IHC-P=1:100-500IHC-F=1:100-500IF=1:50-200(Paraffin sections need to do antigen repair)not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
Product Overview:
Sample: Hela Cell (Human) Lysate at 30 ugPrimary: Anti-KBP (SL9716R) at 1/300 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 72kDObserved band size: 75kDSample: Raji Cell (Human) Lysate at 30 ugPrimary: Anti-KBP (SL9716R) at 1/300 dilutionSecondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilutionPredicted band size: 72kDObserved band size: 75kD
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Unit:
Price: $
Product PDFs
Datasheet:


Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.

Function:
Required for organization of axonal microtubules, andaxonal outgrowth and maintenance during peripheral and centralnervous system development. Regulates mitochondrial transport bymodulating KIF1B motor activity.

Subunit:
Interacts with KIF1B.

Subcellular Location:
Mitochondrion.

Tissue Specificity:
Highly expressed in heart, brain, ovary, testis, spinal cord and all specific brain regions examined. Moderate expressed at intermediate level in all other adult tissues examined, as well as in fetal liver and brain. Not expressed in blood leukocytes.

DISEASE:
Defects in KIAA1279 are the cause of Goldberg-Shprintzenmegacolon syndrome (GOSHS) [MIM:60992]. GOSHS is characterized bymicrocephaly, mental retardation and facial dysmorphism, as well asphenotypes related to Hirschsprung disease syndrome.

Similarity:
Belongs to the KIF1-binding protein family.

SWISS:
Q96EK5

Gene ID:
26128

Database links:

Entrez Gene: 100063227 Horse

Entrez Gene: 26128 Human

Entrez Gene: 7264 Mouse

Entrez Gene: 606294 Rat

Omim: 609367 Human

SwissProt: Q96EK5 Human

SwissProt: Q6ZPU9 Mouse

SwissProt: Q4G074 Rat

Unigene: 279580 Human

Unigene: 258955 Mouse

Unigene: 100975 Rat



Picture

Sample: Hela Cell (Human) Lysate at 30 ug
Primary: Anti-KBP (SL9716R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 72kD
Observed band size: 75kD
Sample: Raji Cell (Human) Lysate at 30 ug
Primary: Anti-KBP (SL9716R) at 1/300 dilution
Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
Predicted band size: 72kD
Observed band size: 75kD
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