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SRP0537

Sigma-Aldrich

BTLA(CD272), FC Fusion

recombinant, expressed in HEK 293 cells

Synonym(s):

CD272

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About This Item

UNSPSC Code:
12352202
NACRES:
NA.26

Pricing and availability is not currently available.

recombinant

expressed in HEK 293 cells

form

frozen liquid

mol wt

40.3 kDa

UniProt accession no.

shipped in

dry ice

storage temp.

−70°C

Gene Information

human ... BTLA(151888)

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1 of 4

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SAB1412471SAB1412666SAB1412667
Gene Information

human ... RUNX1(861)

Gene Information

human ... RUNX1(861)

Gene Information

human ... RUNX2(860)

Gene Information

human ... RUNX2(860)

clone

3A8, monoclonal

clone

3A1, monoclonal

clone

1D2, monoclonal

clone

3F5, monoclonal

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

species reactivity

human

species reactivity

human

species reactivity

human

species reactivity

human

biological source

mouse

biological source

mouse

biological source

mouse

biological source

mouse

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

General description

Human B- and T-lymphocyte attenuator (BTLA)-Fc fusion protein, also known as CD272, GenBank Accession No. NM_181780, a.a. 31-150, expressed in a HEK293 cell expression system. MW = 40.3 kDa (monomer). This protein runs at a higher apparent M.W. by SDS-PAGE due to glycosylation.

Physical form

Aqueous solution

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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    Regioselective synthesis and biological evaluation of novel bis (2-chloroquinolines).
    Rajesh K, et al.
    Research on Chemical Intermediates, 39(9), 4259-4267 (2013)
    Keith Jones et al.
    Organic & biomolecular chemistry, 1(24), 4380-4383 (2003-12-20)
    The synthesis of the quinoline alkaloid atanine 6, by selective demethylation of the 2,4-dimethoxyquinoline 11 is presented. An alternative demethylation utilising a thiolate anion leads to the regioisomeric 4-hydroxyquinoline 13.
    Ultrasound-promoted synthesis of novel 2-chloroquinolin-4-pyrimidine carboxylate derivatives as potential antibacterial agents.
    Balaji GL, et al.
    Research on Chemical Intermediates, 39(4), 1807-1815 (2013)
    Quinoline alkaloids. Part XIII. A convenient synthesis of furoquinoline alkaloids of the dictamnine type.
    Collins JF, et al.
    Journal of the Chemical Society. Perkin Transactions 1, 94-97 (1973)

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