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Catalog: YT2674
Size
Price
Status
Qty.
200μL
$450.00
In stock

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100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

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Main Information
Target

MC2-R

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

WB, IF, ELISA, IHC

MW

34kD (Observed)

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
WB 1:500-2000; IHC 1:50-300; IF 1:200-1:1000; ELISA 1:2000-20000
Formulation
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Specificity
MC2-R Polyclonal Antibody detects endogenous levels of MC2-R protein.
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
1 mg/ml
MW(Observed)
34kD
Modification
Unmodified
Clonality
Polyclonal
Isotype
IgG
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Antigen&Target Information
Immunogen:
The antiserum was produced against synthesized peptide derived from human ACTHR. AA range:248-297
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Specificity:
MC2-R Polyclonal Antibody detects endogenous levels of MC2-R protein.
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Gene Name:
MC2R
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Protein Name:
Adrenocorticotropic hormone receptor
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Other Name:
MC2R ;
ACTHR ;
Adrenocorticotropic hormone receptor ;
ACTH receptor ;
ACTH-R ;
Adrenocorticotropin receptor ;
Melanocortin receptor 2 ;
MC2-R
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Database Link:
Organism Gene ID SwissProt
Human 4158; Q01718;
Mouse 17200; Q64326;
Background:
MC2R encodes one member of the five-member G-protein associated melanocortin receptor family. Melanocortins (melanocyte-stimulating hormones and adrenocorticotropic hormone) are peptides derived from pro-opiomelanocortin (POMC). MC2R is selectively activated by adrenocorticotropic hormone, whereas the other four melanocortin receptors recognize a variety of melanocortin ligands. Mutations in MC2R can result in familial glucocorticoid deficiency. Alternate transcript variants have been found for this gene. [provided by RefSeq, May 2014],
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Function:
Disease:Defects in MC2R are the cause of glucocorticoid deficiency type 1 (GCCD1) [MIM:202200]; also known as familial glucocorticoid deficiency type 1 (FGD1). GCCD1 is an autosomal recessive disorder due to congenital insensitivity or resistance to adrenocorticotropin (ACTH). It is characterized by progressive primary adrenal insufficiency, without mineralocorticoid deficiency.,Function:Receptor for ACTH. This receptor is mediated by G proteins (G(s)) which activate adenylate cyclase.,similarity:Belongs to the G-protein coupled receptor 1 family.,subunit:Interacts with FALP/MRAP.,tissue specificity:Melanocytes and corticoadrenal tissue.,
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Cellular Localization:
Cell membrane; Multi-pass membrane protein.
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Tissue Expression:
Melanocytes and corticoadrenal tissue.
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Research Areas:
>>cAMP signaling pathway ;
>>Neuroactive ligand-receptor interaction ;
>>Aldosterone synthesis and secretion ;
>>Cortisol synthesis and secretion ;
>>Cushing syndrome
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Catalog: YT2674
Size
Price
Status
Qty.
200μL
$450.00
In stock

0

100μL
$280.00
In stock

0

40μL
$150.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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