Anti-TRPM1 Monoclonal Antibody (H-6E10)

Subcat	Description	Isotype	Antibody Modification	Conjugate	Size	Price	Quantity
ASZ1C1899	Anti-TRPM1 Antibody (H-6E10)	Mouse IgG		None		$460		Add

Subcat

Description

Isotype

Antibody Modification

Conjugate

Size

Price

Quantity

ASZ1C1899

Anti-TRPM1 Antibody (H-6E10)

Mouse IgG

None

$460

Add

Anti-TRPM1 Monoclonal Antibody (H-6E10)
- Product Description:
  
  The Anti-TRPM1 antibody is a mouse monoclonal antibody recommended for immunohistochemistry, immunocytochemistry, western blot, immunoprecipitation and other applications. This antibody specifically targets human TRPM1.
  
  Applications:
  
  Immunohistochemistry, Immunocytochemistry, Western Blot, Immunoprecipitation
  
  Source:
  
  Mouse
  
  Target:
  
  TRPM1
  
  Target Species:
  
  Human
  
  Specificity:
  
  This antibody reacts with human Transient Receptor Potential Cation Channel Subfamily M Member 1 (TRPM1).
  
  Clonality:
  
  Monoclonal
  
  Clone ID:
  
  H-6E10
  
  Purification:
  
  The antibody was purified by affinity chromatography.
  
  Purity:
  
  >95% as determined by SDS-PAGE
  
  Concentration:
  
  1 mg/mL
  
  Form:
  
  Liquid
  
  Formulation:
  
  Contact us for custom product formulation.
  
  Preservative:
  
  0.02% sodium azide
  
  Shipping:
  
  Shipped at 4°C.
  
  Storage:
  
  This antibody can be stored at 2°C-8°C for one month. For longer storage, store at -20°C. Avoid repeated freeze-thaw cycles.
Anti-TRPM1 Monoclonal Antibody (H-6E10) Applications
- Recommended Dilution:
  
  Western Blot: 1:500-1:5000
  Immunohistochemistry: 1:50-1:200
  Immunocytochemistry: 1:50-1:200
  
  Note:
  
  Optimal dilutions/concentrations should be determined by the end user.

Protein Name

Transient receptor potential cation channel subfamily M member 1

Introduction

This gene encodes a member of the transient receptor potential melastatin subfamily of transient receptor potential ion channels. The encoded protein is a calcium permeable cation channel that is expressed in melanocytes and may play a role in melanin synthesis. Specific mutations in this gene are the cause autosomal recessive complete congenital stationary night blindness-1C. The expression of this protein is inversely correlated with melanoma aggressiveness and as such it is used as a prognostic marker for melanoma metastasis. Alternate splicing results in multiple transcript variants.

Alternative Names

CSNB1C; LTRPC1; MLSN1

Gene ID

4308

UniProt

Q7Z4N2

Related Disease

Night blindness, congenital stationary, 1C (CSNB1C)

Subcellular Location

Cell membrane

Cell Line Specificity

Cancer enriched