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Key Documents

07-861

Sigma-Aldrich

Anti-phospho-PDGFRα (Tyr742) Antibody

Upstate®, from rabbit

Synonym(s):

CD140A, MGC74795, PDGFR2, platelet-derived growth factor receptor alpha

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

rabbit

Quality Level

100

antibody form

affinity purified immunoglobulin

antibody product type

primary antibodies

clone

polyclonal

purified by

affinity chromatography

species reactivity

mouse, human

manufacturer/tradename

Upstate®

technique(s)

western blot: suitable

isotype

IgG

NCBI accession no.

NM_006206.3

UniProt accession no.

P16234
Q9UD28

shipped in

dry ice

target post-translational modification

phosphorylation (pTyr742)

Gene Information

human ... PDGFRA(5156)

General description

The previously assigned protein identifier Q9UD28 has been merged into P16234. Full details can be found on the UniProt database.

Specificity

Predicted to cross-react with rat based on 100% sequence similarity, but has not been tested.
Recognizes human phospho-PDGFRα (Tyr742). Mouse PDGFRα that is phosphorylated on Tyrosine 742. Rat is predicted to react based on sequence homology.

Immunogen

Peptide corresponding to amino acid region encompassing the human phospho-PDGFRα (Tyr742).

Application

Anti-phospho-PDGFRα (Tyr742) Antibody is an antibody against phospho-PDGFRα (Tyr742) for use in WB.

Quality

Routinely evaluated by immunoblot.

Target description

170-185 kDA

Legal Information

UPSTATE is a registered trademark of Merck KGaA, Darmstadt, Germany

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Markus Zilker et al.
Drug testing and analysis, 11(7), 1065-1075 (2019-03-27)
For assurance of the quality of active pharmaceutical ingredients (APIs) used for manufacturing medicines, the analytical requirements of the European Pharmacopoeia serve as a guideline and have a binding character. Within a particular timeframe, an API is considered to comply

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