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SH2-B Antibody (E-8): sc-393395

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  • SH2-B Antibody (E-8) is a mouse monoclonal IgG1 κ SH2-B antibody, cited in 1 publications, provided at 200 µg/ml
  • raised against amino acids 334-422 mapping within an internal region of SH2-B of human origin
  • SH2-B Antibody (E-8) is recommended for detection of SH2-B of human origin by WB, IP, IF and ELISA
  • Anti-SH2-B Antibody (E-8) is available conjugated to agarose for IP; HRP for WB, IHC(P) and ELISA; and to either phycoerythrin or FITC for IF, IHC(P) and FCM
  • also available conjugated to Alexa Fluor® 488, Alexa Fluor® 546, Alexa Fluor® 594 or Alexa Fluor® 647 for WB (RGB), IF, IHC(P) and FCM, and for use with RGB fluorescent imaging systems, such as iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • also available conjugated to Alexa Fluor® 680 or Alexa Fluor® 790 for WB (NIR), IF and FCM; for use with Near-Infrared (NIR) detection systems, such as LI-COR®Odyssey®, iBright™ FL1000, FluorChem™, Typhoon, Azure and other comparable systems
  • m-IgG1 BP-HRP and m-IgGκ BP-HRP are the preferred secondary detection reagents for SH2-B Antibody (E-8) for WB applications. These reagents are now offered in bundles with SH2-B Antibody (E-8) (see ordering information below).
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SH2-B Antibody (E-8) is a mouse monoclonal IgG1 kappa light chain antibody that detects SH2-B protein of human origin by western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). SH2-B (E-8) antibody is available in both non-conjugated and various conjugated forms, including agarose, horseradish peroxidase (HRP), phycoerythrin (PE), fluorescein isothiocyanate (FITC), and multiple Alexa Fluor® conjugates. SH2-B protein, also known as SH2B1 or PSM, is a 756 amino acid protein that plays a crucial role in the signaling network, particularly in regulating cell shape and movement, which is vital for processes such as cell migration and tissue development. SH2-B protein belongs to the APS family of adapter proteins, characterized by a pleckstrin homology (PH) domain, an SH2 domain, and a tyrosine phosphorylation site, which are essential for signal transduction. SH2-B protein is alternatively spliced to produce three distinct isoforms—SH2-B α, β, and γ—that share a common N-terminal sequence, including the PH domain, SH2 domain, and several proline-rich motifs. These domains enable SH2-B protein to shuttle between the nucleus and cytoplasm, facilitating cellular signaling. SH2-B protein is widely expressed, with highest levels found in skeletal muscle and ovary, and undergoes tyrosine phosphorylation in response to receptor kinase stimulation, further underscoring its importance in cellular communication and response mechanisms.

For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

SH2-B Antibody (E-8) References:

  1. SH2-B is required for nerve growth factor-induced neuronal differentiation.  |  Rui, L., et al. 1999. J Biol Chem. 274: 10590-4. PMID: 10187854
  2. Identification of SH2-bbeta as a potent cytoplasmic activator of the tyrosine kinase Janus kinase 2.  |  Rui, L. and Carter-Su, C. 1999. Proc Natl Acad Sci U S A. 96: 7172-7. PMID: 10377387
  3. APS, an adapter protein with a PH and SH2 domain, is a substrate for the insulin receptor kinase.  |  Ahmed, Z., et al. 1999. Biochem J. 341 (Pt 3): 665-8. PMID: 10417330
  4. SH2-B, a membrane-associated adapter, is phosphorylated on multiple serines/threonines in response to nerve growth factor by kinases within the MEK/ERK cascade.  |  Rui, L., et al. 1999. J Biol Chem. 274: 26485-92. PMID: 10473609
  5. Differential binding to and regulation of JAK2 by the SH2 domain and N-terminal region of SH2-bbeta.  |  Rui, L., et al. 2000. Mol Cell Biol. 20: 3168-77. PMID: 10757801
  6. Regions of the JAK2 tyrosine kinase required for coupling to the growth hormone receptor.  |  Frank, SJ., et al. 1995. J Biol Chem. 270: 14776-85. PMID: 7540178
  7. Identification of SH2-Bbeta as a substrate of the tyrosine kinase JAK2 involved in growth hormone signaling.  |  Rui, L., et al. 1997. Mol Cell Biol. 17: 6633-44. PMID: 9343427
  8. Platelet-derived growth factor (PDGF) stimulates the association of SH2-Bbeta with PDGF receptor and phosphorylation of SH2-Bbeta.  |  Rui, L. and Carter-Su, C. 1998. J Biol Chem. 273: 21239-45. PMID: 9694882

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

SH2-B Antibody (E-8)

sc-393395
200 µg/ml
$322.00

SH2-B Antibody (E-8): m-IgGκ BP-HRP Bundle

sc-523928
200 µg Ab, 40 µg BP
$361.00

SH2-B Antibody (E-8): m-IgG1 BP-HRP Bundle

sc-533626
200 µg Ab; 20 µg BP
$361.00

SH2-B Antibody (E-8) AC

sc-393395 AC
500 µg/ml, 25% agarose
$424.00

SH2-B Antibody (E-8) HRP

sc-393395 HRP
200 µg/ml
$322.00

SH2-B Antibody (E-8) FITC

sc-393395 FITC
200 µg/ml
$336.00

SH2-B Antibody (E-8) PE

sc-393395 PE
200 µg/ml
$349.00

SH2-B Antibody (E-8) Alexa Fluor® 488

sc-393395 AF488
200 µg/ml
$364.00

SH2-B Antibody (E-8) Alexa Fluor® 546

sc-393395 AF546
200 µg/ml
$364.00

SH2-B Antibody (E-8) Alexa Fluor® 594

sc-393395 AF594
200 µg/ml
$364.00

SH2-B Antibody (E-8) Alexa Fluor® 647

sc-393395 AF647
200 µg/ml
$364.00

SH2-B Antibody (E-8) Alexa Fluor® 680

sc-393395 AF680
200 µg/ml
$364.00

SH2-B Antibody (E-8) Alexa Fluor® 790

sc-393395 AF790
200 µg/ml
$364.00

I am using the LiCor/Odyssey system. Which secondary antibody do you recommend using with SH2-B (E-8): sc-393395?

Asked by: DefinitelyNotMatt
We recommend using one of our our exclusive Mouse IgG Binding Proteins conjugated to CFL 680 or CFL 790. They are suitable for use with Near-Infrared (NIR) detection systems, such as LI-COR/Odyssey and other comparable systems. A complete list of available binding proteins is available on our website here: https://www.scbt.com/scbt/browse/support-products-mouse-igg-binding-proteins/_/N-ecrety
Answered by: Technical Support
Date published: 2017-02-27
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Rated 5 out of 5 by from Immunoblot of the endogenous SH2B1 in PC12 cellsAnti-SH2B1 (E8) against aa 334-432 of human SH2B1 (sc.393395) PC12 cells stably expressing GFP tag (only endogenous SH2B1 present). Treated ± NGF (100 ng/ml), cells lysed in RIPA buffer (1% Triton X100). Load 40 ul on minigel. Immunoblot Block with 3% BSA in TBS-1% tween Blot anti-SH2B1 (E8) (1/250 dilution) 2o antibody mIGGkBP-HRP (sc) (1/1000) Nice SH2B1 signal detected with NGF-dependent shift in migration. Band at 90 kDa in absence of NGF. Band at 100 kDa in sample treated with NGF. When PC12 cells stably expressing GFP-SH2B1 beta were used, a dark band was detected at ~125 kDa which was not detected in PC12 expressing GFP alone. When human SH2B1, rat SH2B1, or mouse SH2B1 were expressed in 293T cells, the human SH2B1 and the rat SH2B1 were detected by the (E8) SH2B1 antibody. Mouse SH2B1 was not recognized. A study using 293T cells expressing SH2B1 with various truncations demonstrated that the (E8) SH2B1 antibody recognizes aa 269-397 of SH2B1. Since anti-SH2B1 (E8) was prepared against aa 334-432, from a Clustal W plot for human, rat and mouse the region between aa 334 and 397, the human sequence differs from the mouse sequence at aa 356, 359, 362, and 383. It is likely the epitope for anti-SH2B1 (E8) includes some of these residues.
Date published: 2018-08-23
Rated 5 out of 5 by from Very good Western blot data of SH2Very good Western blot data of SH2-B expression in SJRH30, ES-2 and OV-90 whole cell lysates. -SCBT QC
Date published: 2013-10-10
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SH2-B Antibody (E-8) is rated 5.0 out of 5 by 2.
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