PIPA558237

GBE1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA558237-Each-of-1 In Stock ₹ 48,905.50

PIPA558237 - Each of 1

₹ 48,905.50

In Stock

Quantity

1

Base Price: ₹ 48,905.50

GST (18%): ₹ 8,802.99

Total Price: ₹ 57,708.49

Antigen

GBE1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

GBE1

Gene Alias

1,4-alpha-glucan-branching enzyme; 2310045H19Rik; 2810426P10Rik; amylo-(1,4 to 1,6) transglucosidase; amylo-(1,4 to 1,6) transglycosylase; APBD; Brancher enzyme; D16Ertd536e; GBE; GBE1; glucan (1,4-alpha-), branching enzyme 1; glycogen branching enzyme; glycogen-branching enzyme; GSD4

Host Species

Rabbit

Purification Method

Antigen affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

2632, 288333

Content And Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Form

Liquid

Applications

Immunohistochemistry, Western Blot

Concentration

0.1 mg/mL

Formulation

PBS with 40% glycerol and 0.02% sodium azide; pH 7.2

Gene Accession No.

Q04446

Gene Symbols

GBE1

Immunogen

Recombinant protein corresponding to Human GBE1

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Immunogen sequence: GENEGGIDKF SRGYESFGVH RCADGGLYCK EWAPGAEGVF LTGDFNGWNP FSYPYKKLDY GKWELYIPPK QNKSVLVP Highest antigen sequence identity to the following orthologs: Mouse - 88%, Rat - 87%
  • GBE1 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).