MA191039

Protein APC Monoclonal Antibody (FE9), Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 MA191039-Each-of-1 In Stock ₹ 50,507.50

MA191039 - Each of 1

₹ 50,507.50

In Stock

Quantity

1

Base Price: ₹ 50,507.50

GST (18%): ₹ 9,091.35

Total Price: ₹ 59,598.85

Antigen

Protein APC

Classification

Monoclonal

Concentration

0.1 mg/mL

Formulation

0.05M sodium phosphate with 0.2% gelatin and 0.1% sodium azide; pH 7.5

Gene Accession No.

P25054, P70478, Q61315

Gene Symbols

Apc

Immunogen

synthetic peptide corresponding to the N-terminal 35 amino acid residues of APC.

Quantity

50 μg

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG1

Applications

Western Blot

Clone

FE9

Conjugate

Unconjugated

Gene

Apc

Gene Alias

adenomatosis polyposis coli; adenomatosis polyposis coli tumor suppressor; adenomatous polyposis coli; adenomatous polyposis coli protein; AI047805; APC; APC, WNT signaling pathway regulator; AU020952; AW124434; BTPS2; CC1; Deleted in polyposis 2.5; DP2; DP2.5; DP3; FAP; FPC; GS; mAPC; Min; multiple intestinal neoplasia; PPP1R46; Protein APC; protein phosphatase 1, regulatory subunit 46; RATAPC; truncated adenomatosis polyposis coli; WNT signaling pathway regulator

Host Species

Mouse

Purification Method

Protein G

Regulatory Status

RUO

Gene ID (Entrez)

11789, 24205, 324

Content And Storage

4° C, do not freeze

Form

Liquid

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Description

  • Reacts with all full length and truncated APC proteins
  • MA1-91039 has been successfully used in Western blot applications, where a band of approximately 312 kDa is predicted to be detected
  • Suggested positive controls for this product are HCT116 cells for p300 and SW480 cells for truncated APC (p147)
  • This gene encodes a tumor suppressor protein that acts as an antagonist of the Wnt signaling pathway
  • It is also involved in other processes including cell migration and adhesion, transcriptional activation, and apoptosis
  • Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy
  • Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product.