pan Cadherin Rabbit Monoclonal Antibody

pan Cadherin Rabbit Monoclonal Antibody

Cat: AMRe87400
Size:50μL Price:$168
Size:100μL Price:$300
Application:WB,IHC,ICC/IF

Reactivity:Human
Conjugate:Unconjugated
Optional conjugates: Biotin, FITC (free of charge).
See other 26 conjugates.

Gene Name:pan Cadherin
Category: Recombinant Monoclonal Antibody Tags: , , , , ,

Summary

Production Name

pan Cadherin Rabbit Monoclonal Antibody

Description

Recombinant rabbit monoclonal antibody

Host

Rabbit

Application

WB,IHC,ICC/IF

Reactivity

Human

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

IgG

Clonality

Monoclonal

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% protective protein. Stable for 12 months from date of receipt.

Purification

Affinity Purification

 

Immunogen

Gene Name

pan Cadherin

Alternative Names

CDHP; HJMD; PCAD

Gene ID

1001

SwissProt ID

P22223

 

Application

Dilution Ratio

WB 1:500-1:2000,IHC 1:100-1:200,ICC/IF 1:20-1:50

Molecular Weight

Calculated MW:91 kDa; Observed MW:120 kDa

 

Background

This gene encodes a classical cadherin of the cadherin superfamily. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature glycoprotein. This calcium-dependent cell-cell adhesion protein is comprised of five extracellular cadherin repeats, a transmembrane region and a highly conserved cytoplasmic tail. This gene is located in a gene cluster in a region on the long arm of chromosome 16 that is involved in loss of heterozygosity events in breast and prostate cancer. In addition, aberrant expression of this protein is observed in cervical adenocarcinomas. Mutations in this gene are associated with hypotrichosis with juvenile macular dystrophy and ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome (EEMS). [provided by RefSeq, Nov 2015]

 

Research Area

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