KIF1B (Phospho Ser1487) Rabbit pAb

-YP1379

Catalog: YP1379
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$340.00
3 weeks

0

50μL
$190.00
3 weeks

0

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Collected

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Main Information
Target

KIF1B Phospho Ser1487

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB, IHC, ELISA

MW

200kD (Observed)

Conjugate/Modification


phosphate

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; IHC 1:50-300; ELISA 1:2000-20000
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
This antibody detects endogenous levels of Human KIF1B (phospho-Ser1487)
Purification
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Storage
-15°C to -25°C/1 year (Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
200kD
Modification
phosphate
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
Synthesized phosho peptide around human KIF1B (Ser1487)
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Specificity:
This antibody detects endogenous levels of Human KIF1B (phospho-Ser1487)
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Gene Name:
KIF1B KIAA0591 KIAA1448
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Protein Name:
KIF1B (Ser1487)
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Other Name:
Kinesin-like protein KIF1B ;
Klp ;
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Database Link:
Organism Gene ID SwissProt
Human 23095; O60333;
Mouse 16561; Q60575;
Rat 117548; O88658;
Background:
This gene encodes a motor protein that transports mitochondria and synaptic vesicle precursors. Mutations in this gene cause Charcot-Marie-Tooth disease , type 2A1. [provided by RefSeq , Jul 2008] ,
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Function:
Disease:Defects in KIF1B are the cause of Charcot-Marie-Tooth disease type 2A1 (CMT2A1) [MIM:118210]. CMT2A1 is a form of Charcot-Marie-Tooth disease , the most common inherited disorder of the peripheral nervous system. Charcot-Marie-Tooth disease is classified in two main groups on the basis of electrophysiologic properties and histopathology: primary peripheral demyelinating neuropathy or CMT1 , and primary peripheral axonal neuropathy or CMT2. Neuropathies of the CMT2 group are characterized by signs of axonal regeneration in the absence of obvious myelin alterations , normal or slightly reduced nerve conduction velocities , and progressive distal muscle weakness and atrophy. ,Function:Motor for anterograde transport of mitochondria. Has a microtubule plus end-directed motility. ,similarity:Belongs to the kinesin-like protein family. ,similarity:Belongs to the kinesin-like protein family. Unc-104 subfamily. ,similarity:Contains 1 FHA domain. ,similarity:Contains 1 kinesin-motor domain. ,similarity:Contains 1 PH domain. ,subunit:Interacts with KBP. ,tissue specificity:Isoform 3 is abundant in the skeletal muscle. It is also expressed in fetal brain , lung and kidney , and adult heart , placenta , testis , ovary and small intestine. Isoform 2 is abundant in the brain and also expressed in fetal heart , lung , liver and kidney , and adult skeletal muscle , placenta , liver , kidney , heart , spleen , thymus , prostate , testis , ovary , small intestine , colon and pancreas. ,
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Cellular Localization:
Cytoplasm , cytoskeleton. Mitochondrion . Cell projection , axon .; [Isoform 1]: Cytoplasmic vesicle , secretory vesicle , synaptic vesicle .
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Catalog: YP1379
Size
Price
Status
Qty.
200μL
$600.00
3 weeks

0

100μL
$340.00
3 weeks

0

50μL
$190.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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