89-934-202

GPC3 Mouse anti-Human, Clone: 1G12, Abnova™

Manufacturer: Abnova Corporation

Select a Size

Pack Size SKU Availability Price
Each of 1 89-934-202-Each-of-1 In Stock ₹ 67,640.00

89-934-202 - Each of 1

₹ 67,640.00

In Stock

Quantity

1

Base Price: ₹ 67,640.00

GST (18%): ₹ 12,175.20

Total Price: ₹ 79,815.20

Antigen

GPC3

Classification

Monoclonal

Conjugate

Unconjugated

Dilution

Flow Cytometry (0.5-1 ug/106cells in 0.1 mL) Immunofluorescence (0.5-1 ug/mL) Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (0.5-1 ug/mL) The optimal working dilution should be determined by the end user.

Gene Alias

DGSX/OCI-5/SDYS/SGB/SGBS/SGBS1

Host Species

Mouse

Purification Method

Protein A/G purification

Regulatory Status

RUO

Gene ID (Entrez)

2719

Content And Storage

Store at 4°C.

Isotype

IgG1 κ

Applications

Flow Cytometry, Immunofluorescence, Immunohistochemistry (PFA fixed)

Clone

1G12

Description

Mouse monoclonal antibody raised against partial recombinant human GPC3.

Formulation

In 1mM PBS (0.05% BSA, 0.05% sodium azide).

Gene Symbols

GPC3

Immunogen

Recombinant protein corresponding to amino acids 511-580 of human GPC3.

Quantity

100 μg

Primary or Secondary

Primary

Target Species

Human

Form

Liquid

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Description

  • Cell surface heparan sulfate proteoglycans are composed of a membrane-associated protein core substituted with a variable number of heparan sulfate chains
  • Members of the glypican-related integral membrane proteoglycan family (GRIPS) contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol linkage
  • These proteins may play a role in the control of cell division and growth regulation
  • The protein encoded by this gene can bind to and inhibit the dipeptidyl peptidase activity of CD26, and it can induce apoptosis in certain cell types
  • Deletion mutations in this gene are associated with Simpson-Golabi-Behmel syndrome, also known as Simpson dysmorphia syndrome
  • Alternative splicing results in multiple transcript variants
  • [provided by RefSeq]