U-Blot® TROP-2 Rabbit mAb

U-Blot® TROP-2 Rabbit mAb
U-Blot® TROP-2 Rabbit mAb
$268.00
Size:50μL
SKU: WR5071-50

Catalog No.: WR5071

Specification: 50μL/100μL

Stock: In stock

U-Blot® TROP-2 Rabbit mAb Learn more

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Product information

Product detailsSpecificationsQ & AEducation

Background：This intronless gene encodes a carcinoma-associated antigen. This antigen is a cell surface receptor that transduces calcium signals. Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy.[provided by RefSeq, Dec 2009],

Product Overview

Catalog No.
WR5071
SKU
WR5071-50
Category
Rabbit mAbs
Product Type
Other
Size
50μL/100μL
Stock Status
In stock
Available Stock
20
Minimum Order Quantity
1

Storage & Compliance

Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
Research Use Only
Yes

Additional Specifications

Target
TROP-2
Reactivity
Human,Mouse,Rat
Application
WB,IHC,IF,ELISA
MW(Calculated)
36kD
MW(Observed)
45-65kD
Host Species
Rabbit
Isotype
IgG,Kappa
Conjugate/Modification
Unmodified
Modification site
--
Recommended Dilution Ratio
IHC 1:200-1:1000;WB 1:10000-1:50000;IF 1:200-1:1000;ELISA 1:5000-1:20000;
Form
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Source
--
Purification
Protein A
Purity
--
storageCondition
-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
--
Clonality
Monoclonal
Clone No.
PT1308R
Immunogen
--
Sequence
--
Specificity
Endogenous
Gene Name
TACSTD2
Protein Name
Tumor-associated calcium signal transducer 2
Other Name
TACSTD2;GA733-1;M1S1;TROP2;Tumor-associated calcium signal transducer 2;Cell surface glycoprotein Trop-2;Membrane component chromosome 1 surface marker 1;Pancreatic carcinoma marker protein GA733-1
Organism-1
Human
Gene ID-1
4070
SwissProt-1
P09758
Organism-2
Mouse
Gene ID-2
56753
SwissProt-2
Q8BGV3
Organism-3
Rat
Gene ID-3
494343
SwissProt-3
Q6P9Z6
Organism-4
--
gene ID-4
--
SwissProt-4
--
Cellular Localization
Disease:Defects in TACSTD2 are the cause of gelatinous drop-like corneal dystrophy (GDLD) [MIM:204870]; also known as lattice corneal dystrophy type III. GDLD is an autosomal recessive disorder characterized by grayish corneal amyloid deposits that cause severe visual impairment.,Function:GA733 tumor-associated antigen gene family may function as growth factor receptors.,PTM:The N-terminus is blocked.,similarity:Contains 1 thyroglobulin type-1 domain.,tissue specificity:Placenta, pancreatic carcinoma cell lines.,

Tech Support

ucallm

01

Documents

Datasheet, COA, SDS, and protocol files can be requested from technical support.

02

Storage & Handling

Storage
-15°C to -25°C/1 year(Do not lower than -25°C)
06

Contact Support

Emailinfo@ucallmlabs.com

Phone+(1)-866-986-9598

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Keywords:Rabbit mAbs