PIPA558236

GBE1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA558236-Each-of-1 In Stock ₹ 49,261.50

PIPA558236 - Each of 1

₹ 49,261.50

In Stock

Quantity

1

Base Price: ₹ 49,261.50

GST (18%): ₹ 8,867.07

Total Price: ₹ 58,128.57

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, 74185

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

0.2 mg/mL

Formulation

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

Gene Accession No.

Q04446, Q9D6Y9

Gene Symbols

GBE1

Immunogen

Recombinant protein corresponding to Human GBE1

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Immunogen sequence: SVLTPFTPVI DRGIQLHKMI RLITHGLGGE GYLNFMGNEF GHPEWLDFPR KGNNESYHYA RRQFHLTDDD LLRYKFLNNF DRDMNRLEER YGWLAA Highest antigen sequence identity to the following orthologs: Mouse - 96%, Rat - 95%
  • 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).