GBE1 Mouse Monoclonal Antibody [Clone ID: OTI1D11]

CAT#: TA500829

GBE1 mouse monoclonal antibody, clone OTI1D11 (formerly 1D11)

Size: 30 ul 100 ul

Formulation: Standard Carrier-Free

Conjugation: Unconjugated Biotin HRP



  View other "OTI1D11" antibodies (4)

Need it in bulk or conjugated?
Get a free quote

【特别福利】购一抗正装产品(≥50ul或≥50ug),免费领10ul抗体试用装

CNY 1,999.00

CNY 2,700.00


货期*
现货

规格
    • 100 ul

Cited in 2 publications.
经常一起买 (4)
Transient overexpression lysate of glucan (1,4-alpha-), branching enzyme 1 (GBE1)
    • 100 ug

CNY 3,080.00


beta Actin Mouse Monoclonal Antibody, Clone OTI1, Loading Control
    • 30 ul

CNY 300.00
CNY 1,430.00


Recombinant protein of human glucan (1,4-alpha-), branching enzyme 1 (GBE1), 20 µg
    • 20 ug

CNY 2,900.00
CNY 6,650.00


Recombinant protein of human glucan (1,4-alpha-), branching enzyme 1 (GBE1), 100 µg
    • 100 ug

CNY 9,998.00

Specifications

Product Data
Clone Name OTI1D11
Applications FC, IF, IHC, IP, WB
Recommend Dilution WB 1:500~2000, IHC 1:50, IF 1:50~100, FLOW 1:100, IP 2ug/500ul
Reactivity Human, Mouse, Rat
Host Mouse
Clonality Monoclonal
Immunogen Full length human recombinant protein of human GBE1 (NP_000149) produced in HEK293T cell.
Formulation PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Concentration 1.1 mg/ml
Purification Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
Conjugation Unconjugated
Storage Condition Store at -20°C as received.
Predicted Protein Size 80.3 kDa
Gene Name 1,4-alpha-glucan branching enzyme 1
Background The protein encoded by this gene is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease). [provided by RefSeq]
Synonyms APBD; GBE; GSD4
Reference Data
Protein Families Druggable Genome
Protein Pathways Metabolic pathways, Starch and sucrose metabolism
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.

Citations (2)

Other Versions

Customer Reviews 
Loading...