Home > Product > Antibody > Rabbit Anti-phospho-IL3RB (Tyr766) antibody
phospho-CSF2RB (Tyr766); IL3RB (phospho Y766); GM-CSF receptor beta chain; Cytokine receptor common subunit beta; CDw131; GM-CSF/IL-3/IL-5 receptor common beta subunit; CSF2RB; IL3RB; IL5RB: GM-CSFrβ.
Cat:
SL5252R
Species Reactivity:
(predicted: Human,Pig,Cow,Horse,Rabbit,Guinea Pig,)
Immunogen:
KLH conjugated Synthesised phosphopeptide derived from human CSF2RB around the phosphorylation site of Tyr766:EG(p-Y)VE
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=1:5000-10000not yet tested in other applications.optimal dilutions/concentrations should be determined by the end user.
Host:
Rabbit
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Unit:
Price: $
Product PDFs
Datasheet:


GM-CSF Receptor Beta is the v subunit of the heterodimeric receptor for colony stimulating factor 2, a cytokine which controls the production, differentiation, and function of granulocytes and macrophages. The encoded protein is a member of the cytokine family of receptors. This gene is found in the pseudoautosomal region (PAR) of the X and Y chromosomes. Six transcript variants encoding five different isoforms have been found for this gene, with some of the isoforms being membrane-bound and others being soluble.

Function:
High affinity receptor for interleukin-3, interleukin-5 and granulocyte-macrophage colony-stimulating factor.

Subunit:
Heterodimer of an alpha and a beta subunit. The beta subunit is common to the IL3, IL5 and GM-CSF receptors. The signaling GM-CSF receptor complex is a dodecamer of two head-to-head hexamers of two alpha, two beta, and two ligand subunits. Interacts with TMEM102; this interaction occurs preferentially in the absence of CSF2. Interacts with LYN.

Subcellular Location:
Membrane; Single-pass type I membrane protein.

Tissue Specificity:
Defects in CSF2RB are the cause of pulmonary surfactant metabolism dysfunction type 5 (SMDP5) [MIM:614370]. SMDP5 is a rare lung disorder due to impaired surfactant homeostasis. It is characterized by alveolar filling with floccular material that stains positive using the periodic acid-Schiff method and is derived from surfactant phospholipids and protein components. Excessive lipoproteins accumulation in the alveoli results in severe respiratory distress.

Post-translational modifications:
May be phosphorylated by LYN.

Similarity:
Belongs to the type I cytokine receptor family. Type 4 subfamily.
Contains 2 fibronectin type-III domains.

SWISS:
P32927

Gene ID:
1439

Database links:

Entrez Gene: 1439 Human

Entrez Gene: 12983 Mouse

Entrez Gene: 12984 Mouse

Omim: 138981 Human

SwissProt: P32927 Human

SwissProt: P26955 Mouse

Unigene: 285401 Human

Unigene: 592192 Human

Unigene: 235324 Mouse



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