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c-Kit/CD117 (Phospho Tyr823) Rabbit pAb

-YP1303

Catalog: YP1303
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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Main Information
Target

CD117 Phospho Tyr823

Host Species

Rabbit

Reactivity

Human, Mouse, Rat

Applications

WB

MW

117kD (Observed)

Conjugate/Modification


phosphate

Detailed Information
Recommended Dilution Ratio
WB 1:1000-2000
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
This antibody detects endogenous levels of Human c-Kit (phospho-Tyr823)
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)
117kD
Modification
phosphate
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
Synthesized phosho peptide around human c-Kit (Tyr823)
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Specificity:
This antibody detects endogenous levels of Human c-Kit (phospho-Tyr823)
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Gene Name:
KIT SCFR
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Protein Name:
c-Kit (Tyr823)
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Other Name:
Mast/stem cell growth factor receptor Kit ;
SCFR ;
Piebald trait protein ;
PBT ;
Proto-oncogene c-Kit ;
Tyrosine-protein kinase Kit ;
p145 c-kit ;
v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog ;
CD antigen CD117 ;
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Database Link:
Organism Gene ID SwissProt
Human 3815; P10721;
Mouse 16590; P05532;
Background:
This gene encodes the human homolog of the proto-oncogene c-kit. C-kit was first identified as the cellular homolog of the feline sarcoma viral oncogene v-kit. This protein is a type 3 transmembrane receptor for MGF (mast cell growth factor , also known as stem cell factor) . Mutations in this gene are associated with gastrointestinal stromal tumors , mast cell disease , acute myelogenous lukemia , and piebaldism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq , Jul 2008] ,
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Function:
Catalytic activity:ATP + a [protein]-L-tyrosine = ADP + a [protein]-L-tyrosine phosphate. ,Disease:Defects in KIT are a cause of gastrointestinal stromal tumor (GIST) [MIM:606764]. ,Disease:Defects in KIT are a cause of piebaldism [MIM:172800]. Piebaldism is an autosomal dominant genetic developmental abnormality of pigmentation characterized by congenital patches of white skin and hair that lack melanocytes. ,Disease:Defects in KIT have been associated with testicular tumors [MIM:273300]. It includes germ cell tumor (GCT) or testicular germ cell tumor (TGCT) . ,Function:This is the receptor for stem cell factor (mast cell growth factor) . It has a tyrosine-protein kinase activity. Binding of the ligands leads to the autophosphorylation of KIT and its association with substrates such as phosphatidylinositol 3-kinase (Pi3K) . ,online information:CD117 entry ,similarity:Belongs to the protein kinase superfamily. Tyr protein kinase family. ,similarity:Belongs to the protein kinase superfamily. Tyr protein kinase family. CSF-1/PDGF receptor subfamily. ,similarity:Contains 1 protein kinase domain. ,similarity:Contains 5 Ig-like C2-type (immunoglobulin-like) domains. ,subunit:Interacts with APS. Interacts with MPDZ (via the tenth PDZ domain) . Interacts with PTPRU. ,
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Cellular Localization:
[Isoform 1]: Cell membrane; Single-pass type I membrane protein.; [Isoform 2]: Cell membrane; Single-pass type I membrane protein.; [Isoform 3]: Cytoplasm . Detected in the cytoplasm of spermatozoa , especially in the equatorial and subacrosomal region of the sperm head. .
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Research Areas:
>>MAPK signaling pathway ;
>>Ras signaling pathway ;
>>Rap1 signaling pathway ;
>>Phospholipase D signaling pathway ;
>>PI3K-Akt signaling pathway ;
>>Hematopoietic cell lineage ;
>>Melanogenesis ;
>>Pathways in cancer ;
>>Acute myeloid leukemia ;
>>Breast cancer ;
>>Central carbon metabolism in cancer
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Catalog: YP1303
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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