PIPA5102717

CHRNB1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5102717-Each-of-1 In Stock ₹ 46,502.50

PIPA5102717 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

CHRNB1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

Chrnb1

Gene Alias

acetylcholine receptor; acetylcholine receptor beta; acetylcholine receptor subunit beta; acetylcholine receptor, nicotinic, beta 1 (muscle); AChR beta; Achr-2; ACHRB; Acrb; cholinergic receptor; cholinergic receptor nicotinic beta 1 subunit; cholinergic receptor nicotinic beta polypeptide 1; cholinergic receptor, nicotinic beta 1; cholinergic receptor, nicotinic, beta 1 (muscle); cholinergic receptor, nicotinic, beta polypeptide 1 (muscle); CHRNB; Chrnb 1; CHRNB1; CMS1D; CMS2A; CMS2C; nAChRB1; RNACRB1; SCCMS

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

1140, 11443, 24261

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide; pH 7.4

Gene Accession No.

P09690, P11230, P25109

Gene Symbols

Chrnb1

Immunogen

A synthesized peptide derived from human CHRNB1(Accession P11230), corresponding to amino acid residues L63-V113.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Antibody detects endogenous levels of total CHRNB1
  • The muscle acetylcholine receptor is composed of five subunits: two alpha subunits and one beta, one gamma, and one delta subunit
  • This gene encodes the beta subunit of the acetylcholine receptor
  • The acetylcholine receptor changes conformation upon acetylcholine binding leading to the opening of an ion-conducting channel across the plasma membrane
  • Mutations in this gene are associated with slow-channel congenital myasthenic syndrome.