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Key Documents

SRP0537

BTLA(CD272), FC Fusion

Name: BTLA(CD272), FC Fusion
Brand: SIGMA

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.

Q7Z6A9

shipped in

dry ice

storage temp.

−70°C

Gene Information

human ... BTLA(151888)

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This Item	SAB1412471	SAB1412666	SAB1412667
SAB1412470 ANTI-RUNX1 antibody produced in mouse	SAB1412471 ANTI-RUNX1 antibody produced in mouse	SAB1412666 ANTI-RUNX2 antibody produced in mouse	SAB1412667 ANTI-RUNX2 antibody produced in mouse
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

GHS07

signalword

Warning

hcodes

H315,H319

pcodes

P305 + P351 + P338

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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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.

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Balaji GL, et al.

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Quinoline alkaloids. Part XIII. A convenient synthesis of furoquinoline alkaloids of the dictamnine type.

Collins JF, et al.

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