CoraLite® Plus 488-conjugated TGF beta 1 Monoclonal antibody

TGF beta 1 Monoclonal Antibody for

Host / Isotype

Mouse / IgG1

Reactivity

Human

Applications

Conjugate

CoraLite® Plus 488 Fluorescent Dye

CloneNo.

1E3E9

Cat no : CL488-69012

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Synonyms

CED, DPD1, LAP, NeutraKine® TGF beta 1, TGF ?1, TGF beta 1, TGFB, TGFB1, TGFbeta, TGF-beta1



Planning an IHC experiment? We recommend our IHCeasy TGF beta 1 Ready-To-Use IHC Kit. TGF beta 1 primary antibody included.
For other applications, we recommend the unconjugated version of this antibody, 69012-1-Ig

产品信息

CL488-69012 targets TGF beta 1 in applications and shows reactivity with Human samples.

Tested Applications Application Description
Tested Reactivity Human
Immunogen TGF beta 1 fusion protein HZ-1011 种属同源性预测
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Full Name transforming growth factor, beta 1
Synonyms CED, DPD1, LAP, NeutraKine® TGF beta 1, TGF ?1, TGF beta 1, TGFB, TGFB1, TGFbeta, TGF-beta1
Gene Symbol TGFB1
Gene ID (NCBI) 7040
Conjugate CoraLite® Plus 488 Fluorescent Dye
Excitation/Emission Maxima Wavelengths493 nm / 522 nm
Form Liquid
Purification MethodProtein G purification
Storage Buffer PBS with 50% Glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
Storage ConditionsStore at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

TGFB, also named as LAP and TGFB1, is a multifunctional peptide that controls proliferation, differentiation, and other functions in many cell types. TGFB acts synergistically with TGFA in inducing transformation. It also acts as a negative autocrine growth factor. Dysregulation of TGFB activation and signaling may result in apoptosis. Many cells synthesize TGFB and almost all of them have specific receptors for it. TGFB positively and negatively regulates many other growth factors. It plays an important role in bone remodeling as it is a potent stimulator of osteoblastic bone formation, causing chemotaxis, proliferation and differentiation in committed osteoblasts. It is highly expressed in bone. Mutation of TGFB are the cause of Camurati-Engelmann disease (CED) which known as progressive diaphyseal dysplasia 1 (DPD1).