Description:

Size: 100ul

Catalog no.: bs-2101R-A594

Price: 380 EUR

Product details

Modification Site

None

Gene ID Number

57124

Swiss Prot

Q9HCU0

French translation

anticorps

Modification

Unmodified

Clonality

Polyclonal

Target Antigen

TEM1/CD248

Excitation emission

590nm/617nm

Concentration

1ug per 1ul

Immunogen range

280-320/757

Subcellular location

Extracellular

Tested applications

FCM, IF(IHC-P)

Conjugated

Alexa conjugate 1

Conjugated with

ALEXA FLUOR® 594

Crossreactivity

Human, Mouse, Rat

Clone

Polyclonal antibody

Purification

Purified by Protein A.

Category

Conjugated Primary Antibodies

Conjugation

Alexa Fluor,ALEXA FLUOR® 594

Host Organism

Rabbit (Oryctolagus cuniculus)

Recommended dilutions

FCM(1:20-100), IF(IHC-P)(1:50-200)

Also known as

Anti-TEM1/CD248 PAb ALEXA FLUOR 594

Specificity

This is a highly specific antibody against TEM1/CD248.

Long name

TEM1/CD248 Polyclonal Antibody, ALEXA FLUOR 594 Conjugated

Synonyms

TEM1; CD164L1; Endosialin; Tumor endothelial marker 1; CD248

Cross-reactive species details

Due to limited amount of testing and knowledge, not every possible cross-reactivity is known.

Source

This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human TEM 1

Storage conditions

Store this antibody in aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide. Keep refrigerated at 2 to 8 degrees Celcius for up to one year.

Properties

For facs or microscopy Alexa 1 conjugate.If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies. ALEXA FLUOR they should be stored frozen at - 24°C for long term storage and for short term at + 5°C.

Background of the antigen

The transmembrane glycoprotein Tumor endothelial marker 1 (TEM1) is highly expressed in tumor endothelial cells however it is barely detectable on normal endothelial cells. It is believed to play a role in tumor angiogenesis. It is expressed in stromal fibroblasts, metastatic hepatic lesions and during angiogenesis of corpus luteum formation and wound healing. TEM1 is being investigated as a potential target for cancer treatment.