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Mouse Monoclonal AntibodiesCat. No. GAM703892

G6PC Rabbit monoclonal antibody,clone OTIR2H10

Aliasesglucose 6 phosphatasecatalytic subunit
ReactivityHuman
ApplicationsIHC · WB
Host / ClonalityMouse / Monoclonal
Lead timeIn stock · ships in 48h
$169/ 50μlIn stock 200 · Ready to ship
50μl$169
100μl$299

Applications & Recommended Dilution

Applications & DilutionRecommended Dilution
IHC
Recommended dilution1:300-1:1500
Reactivity
Human
Assay
IHC
WB
Recommended dilution1:2000
Reactivity
Human
Assay
WB

Product Images

Product ImagesImages

Product Specifications

SpecificationsProduct Specifications
Core Attributes CORE ATTRIBUTES
Species Reactivity
Human
Applications
IHCWB
Clone name
OTIR2H10
Calculated molecular weight
40.5 kDa
Immunogen
Synthetic peptide (the amino acid sequence is considered to be commercially sensitive) within Human G6PC (NP_000142). The exact sequence is proprietary.
Isotype
IgG
Host species
Mouse
Clonality
Monoclonal
Purification method
Affinity Purification
Uniprot-A
P35575
Recommended Dilution RECOMMENDED DILUTION
WB
1:2000
IHC
1:300-1:1500
Product Properties PRODUCT PROPERTIES
Shipping
They are shipped out with dry ice/blue ice unless customers require otherwise
Storage Condition
Store at -20°C PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.Stable for 12 months from date of receipt.
Formulation
Liquid
Storage Buffer
PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.[provided by RefSeq, Feb 2011]

Storage & Shipping

Storage & ShippingHandling

01Shipping

They are shipped out with dry ice/blue ice unless customers require otherwise

02Storage Condition

Store at -20°C PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.Stable for 12 months from date of receipt.

03Formulation

Liquid

04Storage Buffer

PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.

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