Description:

Size: 100ul

Catalog no.: bs-10489R-A350

Price: 380 EUR

Product details

Virus

hhv

Modification Site

None

Cross-reactive species details

HHV1

Crossreactivity

Virus

Tested applications

IF(IHC-P)

French translation

anticorps

Modification

Unmodified

Clonality

Polyclonal

Concentration

1ug per 1ul

Excitation emission

343nm/442nm

Immunogen range

1200-1235/1235

Conjugated with

ALEXA FLUOR® 350

Recommended dilutions

IF(IHC-P)(1:50-200)

Clone

Polyclonal antibody

Purification

Purified by Protein A.

Conjugation

Alexa Fluor,ALEXA FLUOR 350

Category

Conjugated Primary Antibodies

Host Organism

Rabbit (Oryctolagus cuniculus)

Target Antigen

HHV DNA polymerase catalytic subunit

Also known as

Anti-HHV DNA polymerase catalytic subunit PAb ALEXA FLUOR 350

Synonyms

DPOL_HHV11; DNA polymerase catalytic subunit; UL30; HHV1gp046.

Long name

HHV DNA polymerase catalytic subunit Antibody, ALEXA FLUOR 350 Conjugated

Specificity

This is a highly specific antibody against HHV DNA polymerase catalytic subunit.

Source

This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human Human herpesvirus 1 DNA polymerase catalytic subunit

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.Alexa Fluor 350 conjugates can be used in multi-color flow cytometry with FACS's equipped with a second red laser or red diode.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

Replicates viral genomic DNA. The replication complex is composed of six viral proteins: the DNA polymerase, processivity factor, primase, primase-associated factor, helicase, and ssDNA-binding protein. Additionally, the polymerase contains an intrinsic ribonuclease H (RNase H) activity that specifically degrades RNA/DNA heteroduplexes or duplex DNA substrates in the 5' to 3' direction. Therefore, it can catalyze the excision of the RNA primers that initiate the synthesis of Okazaki fragments at a replication fork during viral DNA replication.