product summary
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company name :
MyBioSource
product type :
antibody
product name :
Polyclonal Antibody to Phospholipase C Beta 4 (PLCb4)
catalog :
MBS2033947
quantity :
0.01 mg
price :
110 USD
clonality :
polyclonal
host :
rabbit
conjugate :
nonconjugated
reactivity :
human
application :
western blot, immunohistochemistry, immunocytochemistry, immunoprecipitation
more info or order :
image
image 1 :
MyBioSource MBS2033947 image 1
Western Blot: Sample: Recombinant protein.
product information
catalog number :
MBS2033947
products type :
Antibody
products full name :
Polyclonal Antibody to Phospholipase C Beta 4 (PLCb4)
products short name :
[Phospholipase C Beta 4]
products name syn :
[PI-PLC; Phospholipase C-beta-4; Phosphoinositide phospholipase C-beta-4; 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4]
other names :
[1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4 isoform a; 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4; 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4; phospholipase C beta 4; Phosphoinositide phospholipase C-beta-4; Phospholipase C-beta-4; PLC-beta-4]
products gene name :
[PLCb4]
other gene names :
[PLCB4; PLCB4; ARCND2; PI-PLC; PLC-beta-4]
clonality :
Polyclonal
isotype :
IgG
host :
Rabbit
reactivity :
Human
specificity :
The antibody is a Rabbit polyclonal antibody raised against PLCb4. It has been selected for its ability to recognize PLCb4 in immunohistochemical staining and western blotting.
purity :
Antigen-specific Affinity Chromatography
form :
Supplied as solution form in 0.01M PBS, pH7.4, containing 0.05% Proclin-300, 50% glycerol
concentration :
200ug/ml
storage stability :
Storage: Avoid repeated freeze/thaw cycles. Store at 4 degree C for frequent use. Aliquot and store at -20 degree C for 12 months. Stability Test: The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37 degree C for 48h, and no obvious degradation and precipitation were observed. The loss rate is less than 5% within the expiration date under appropriate storage condition.
tested application :
WB; IHC; ICC; IP
app notes :
Western blotting: 0.5-2µg/mL. Immunocytochemistry in formalin fixed cells: 5-20µg/mL. Immunohistochemistry in formalin fixed frozen section: 5-20µg/mL. Immunohistochemistry in paraffin section: 5-20µg/mL. Optimal working dilutions must be determined by end user
image1 heading :
Western Blot (WB)
other info1 :
Source: Polyclonal antibody preparation. Traits: Liquid. Immunogen: Recombinant PLCb4 (Ala2~Gln250) expressed in E.coli
other info2 :
Conjugated Antibody: The APC conjugated antibody version of this item is also available as catalog #MBS2073145
ncbi gi num :
289547589
ncbi acc num :
NP_000924.3
ncbi gb acc num :
NM_000933.3
uniprot acc num :
Q15147
ncbi mol weight :
135,845 Da
ncbi pathways :
Adrenergic Signaling In Cardiomyocytes Pathway (908257); Adrenergic Signaling In Cardiomyocytes Pathway (909696); African Trypanosomiasis Pathway (194384); African Trypanosomiasis Pathway (194323); Alzheimer's Disease Pathway (83097); Alzheimer's Disease Pathway (509); Alzheimers Disease Pathway (672448); Amoebiasis Pathway (167324); Amoebiasis Pathway (167191); Calcium Signaling Pathway (83050)
ncbi summary :
The protein encoded by this gene catalyzes the formation of inositol 1,4,5-trisphosphate and diacylglycerol from phosphatidylinositol 4,5-bisphosphate. This reaction uses calcium as a cofactor and plays an important role in the intracellular transduction of many extracellular signals in the retina. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2010]
uniprot summary :
PLCB4: The production of the second messenger molecules diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3) is mediated by activated phosphatidylinositol-specific phospholipase C enzymes. This form has a role in retina signal transduction. Defects in PLCB4 are the cause of auriculocondylar syndrome type 2 (ARCND2). ARCND2 is an autosomal dominant craniofacial malformation syndrome characterized by variable mandibular anomalies, including mild to severe micrognathia, temporomandibular joint ankylosis, cleft palate, and a characteristic ear malformation that consists of separation of the lobule from the external ear, giving the appearance of a question mark (question-mark ear). Other frequently described features include prominent cheeks, cupped and posteriorly rotated ears, preauricular tags, and microstomia. 3 isoforms of the human protein are produced by alternative splicing. Protein type: Carbohydrate Metabolism - inositol phosphate; EC 3.1.4.11; Phospholipase. Chromosomal Location of Human Ortholog: 20p12.3-p12.2. Cellular Component: cytosol; dendrite; nucleus; postsynaptic density; smooth endoplasmic reticulum. Molecular Function: calcium ion binding; phosphoinositide phospholipase C activity; phospholipase C activity; protein binding; signal transducer activity. Biological Process: G-protein coupled receptor signaling pathway; inositol phosphate metabolic process; lipid catabolic process. Disease: Auriculocondylar Syndrome 2
size1 :
0.01 mg
price1 :
110 USD
size2 :
0.02 mg
price2 :
130
size3 :
0.05 mg
price3 :
175
size4 :
0.1 mg
price4 :
225
size5 :
0.2 mg
price5 :
340
size6 :
1 mg
price6 :
800
more info or order :
company information
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-888-627-0165
headquarters: USA
MyBioSource, LLC was orginally founded in Vancouver by three enthusiastic scientists who are passionate about providing the world with the best reagents available. Together, they form a company with a big vision known as MyBioSource. MyBioSource is now located in San Diego, California, USA.

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