anti-hsa-mir-29a RT-PCR Primer Set Antibody, 1 nmol

Category

pcr kit
Raised in

laboratory
Clone

1 vial
Form

pure
Reactivity

Human
Purity

purified
Molecular weight

in kDa
Source

mammalian
Activity

to be determined
Range

broad
Protein number

see ncbi
Application

not determined
Storage

Shipped at 4°C. Upon delivery aliquot and store at -20°C for one year. Avoid freeze/thaw cycles.
Antibody s specifications
Description

This antibody needs to be stored at + 4°C in a fridge short term in a concentrated dilution. Freeze thaw will destroy a percentage in every cycle and should be avoided. Antibody for research use.
Properties

If you buy Antibodies supplied by acr they should be stored frozen at - 24°C for long term storage and for short term at + 5°C. Thermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR.
Group

PCR, polymerase chain reaction, RT-PCR mixes
About

TAQ or Pfu or Pfx or other enzymes are used for polycmerase chain reaction and have different specificity. The mores specific the lower the yield.
French translation

anticorps

Gene target

hsa-mir-29a Primer Set nmol
Short name

anti-hsa-mir-29a RT-PCR Primer Set Antibody, 1 nmol
Technique

Antibody, RT-PCR, anti-, anti, PCR, antibody to, antibodies, antibodies against human proteins, antibodies for, The polymerase chain reaction (PCR) amplifies the DNA in your sample. For real time PCR the cycle threshold Ct values willneed to be set before the experiment. Than the RT-PCR starts from RNA and real time PCR quantitates the cDNA so the RNA in the sample on given time of the experiment.
Isotype

reagent
Species

human
Alternative name

Antibody tohsa-mir-29a Reverse transcription PCR test kit Primer Set (antibody to-), 1 nmol
Alternative technique

antibodies, rtpcrkits, pcr-sequence, dna-amplification
Tissue

set

Name

Polymerase Chain Reaction
Concept

Scope note: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
Tree numbers
- E05.393.620.500
Qualifiers

ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data